Screens in fly and beetle reveal vastly divergent gene sets required for developmental processes. 
 PMID:35135533
                                    
                                
                                    FAIR data representation in times of eScience: a comparison of instance-based and class-based semantic representations of empirical data using phenotype descriptions as example. 
 PMID:34823588
                                    
                                
                                    A starting guide to root ecology: strengthening ecological concepts and standardising root classification, sampling, processing and trait measurements. 
 PMID:34608637
                                    
                                
                                    Planarian Anatomy Ontology: a resource to connect data within and across experimental platforms. 
 PMID:34318308
                                    
                                
                                    Applying FAIR Principles to Plant Phenotypic Data Management in GnpIS. 
 PMID:33313522
                                    
                                
                                    Transforming the study of organisms: Phenomic data models and knowledge bases. 
 PMID:33232313
                                    
                                
                                    Predicting candidate genes from phenotypes, functions and anatomical site of expression. 
 PMID:33051643
                                    
                                
                                    Semantic similarity and machine learning with ontologies. 
 PMID:33049044
                                    
                                
                                    BiPOm: a rule-based ontology to represent and infer molecule knowledge from a biological process-centered viewpoint. 
 PMID:32703160
                                    
                                
                                    Semantic characterization of adverse outcome pathways. 
 PMID:32278258
                                    
                                
                                    Automated Methods Enable Direct Computation on Phenotypic Descriptions for Novel Candidate Gene Prediction. 
 PMID:31998331
                                    
                                
                                    The Monarch Initiative in 2019: an integrative data and analytic platform connecting phenotypes to genotypes across species. 
 PMID:31701156
                                    
                                
                                    A Logical Model of Homology for Comparative Biology. 
 PMID:31596473
                                    
                                
                                    Phenotype annotation with the ontology of microbial phenotypes (OMP). 
 PMID:31307550
                                    
                                
                                    PathoPhenoDB, linking human pathogens to their phenotypes in support of infectious disease research. 
 PMID:31160594
                                    
                                
                                    Trait ontology analysis based on association mapping studies bridges the gap between crop genomics and Phenomics. 
 PMID:31159731
                                    
                                
                                    Review: New sensors and data-driven approaches-A path to next generation phenomics. 
 PMID:31003608
                                    
                                
                                    Quantitative evaluation of ontology design patterns for combining pathology and anatomy ontologies. 
 PMID:30858527
                                    
                                
                                    Annotation of phenotypes using ontologies: a gold standard for the training and evaluation of natural language processing systems. 
 PMID:30576485
                                    
                                
                                    Ontology-based semantic mapping of chemical toxicities. 
 PMID:30468866
                                    
                                
                                    Biomedical ontology alignment: an approach based on representation learning. 
 PMID:30111369
                                    
                                
                                    Discovering Health Benefits of Phytochemicals with Integrated Analysis of the Molecular Network, Chemical Properties and Ethnopharmacological Evidence. 
 PMID:30096807
                                    
                                
                                    Creating a Structured AOP Knowledgebase via Ontology-Based Annotations. 
 PMID:30057931
                                    
                                
                                    High-throughput mouse phenomics for characterizing mammalian gene function. 
 PMID:29626206
                                    
                                
                                    Where to search top-K biomedical ontologies? 
 PMID:29579141
                                    
                                
                                    Tackling the challenges of matching biomedical ontologies. 
 PMID:29335022
                                    
                                
                                    Automated Integration of Trees and Traits: A Case Study Using Paired Fin Loss Across Teleost Fishes. 
 PMID:29325126
                                    
                                
                                    Improving the interoperability of biomedical ontologies with compound alignments. 
 PMID:29316968
                                    
                                
                                    Integrating phenotype ontologies with PhenomeNET. 
 PMID:29258588
                                    
                                
                                    Semantic prioritization of novel causative genomic variants. 
 PMID:28414800
                                    
                                
                                    The anatomy of phenotype ontologies: principles, properties and applications. 
 PMID:28387809
                                    
                                
                                    Drosophila and genome-wide association studies: a review and resource for the functional dissection of human complex traits. 
 PMID:28151408
                                    
                                
                                    The Monarch Initiative: an integrative data and analytic platform connecting phenotypes to genotypes across species. 
 PMID:27899636
                                    
                                
                                    The Zebrafish Model Organism Database: new support for human disease models, mutation details, gene expression phenotypes and searching. 
 PMID:27899582
                                    
                                
                                    The flora phenotype ontology (FLOPO): tool for integrating morphological traits and phenotypes of vascular plants. 
 PMID:27842607
                                    
                                
                                    Modeling biochemical pathways in the gene ontology. 
 PMID:27589964
                                    
                                
                                    A scientist's guide for submitting data to ZFIN. 
 PMID:27443940
                                    
                                
                                    The cellular microscopy phenotype ontology. 
 PMID:27195102
                                    
                                
                                    Data Sources for Trait Databases: Comparing the Phenomic Content of Monographs and Evolutionary Matrices. 
 PMID:27191170
                                    
                                
                                    Capturing phenotypes for precision medicine. 
 PMID:27148566
                                    
                                
                                    Reporting phenotypes in mouse models when considering body size as a potential confounder. 
 PMID:26865945
                                    
                                
                                    PhenoMiner: from text to a database of phenotypes associated with OMIM diseases. 
 PMID:26507285
                                    
                                
                                    Phenoscape: Identifying Candidate Genes for Evolutionary Phenotypes. 
 PMID:26500251
                                    
                                
                                    The digital revolution in phenotyping. 
 PMID:26420780
                                    
                                
                                    Applications of comparative evolution to human disease genetics. 
 PMID:26338499
                                    
                                
                                    Use of model organism and disease databases to support matchmaking for human disease gene discovery. 
 PMID:26269093
                                    
                                
                                    The iBeetle large-scale RNAi screen reveals gene functions for insect development and physiology. 
 PMID:26215380
                                    
                                
                                    Development of an Ontology for Periodontitis. 
 PMID:26140188
                                    
                                
                                    The Human Phenotype Ontology: Semantic Unification of Common and Rare Disease. 
 PMID:26119816
                                    
                                
                                    Disease insights through cross-species phenotype comparisons. 
 PMID:26092691
                                    
                                
                                    Analysis of the human diseasome using phenotype similarity between common, genetic, and infectious diseases. 
 PMID:26051359
                                    
                                
                                    Toward Synthesizing Our Knowledge of Morphology: Using Ontologies and Machine Reasoning to Extract Presence/Absence Evolutionary Phenotypes across Studies. 
 PMID:26018570
                                    
                                
                                    Moving the mountain: analysis of the effort required to transform comparative anatomy into computable anatomy. 
 PMID:25972520
                                    
                                
                                    TermGenie - a web-application for pattern-based ontology class generation. 
 PMID:25937883
                                    
                                
                                    Linking gene expression to phenotypes via pathway information. 
 PMID:25901272
                                    
                                
                                    The role of ontologies in biological and biomedical research: a functional perspective. 
 PMID:25863278
                                    
                                
                                    eNanoMapper: harnessing ontologies to enable data integration for nanomaterial risk assessment. 
 PMID:25815161
                                    
                                
                                    Supporting the annotation of chronic obstructive pulmonary disease (COPD) phenotypes with text mining workflows. 
 PMID:25789153
                                    
                                
                                    An ontology approach to comparative phenomics in plants. 
 PMID:25774204
                                    
                                
                                    Similarity-based search of model organism, disease and drug effect phenotypes. 
 PMID:25763178
                                    
                                
                                    A bioinformatics expert system linking functional data to anatomical outcomes in limb regeneration. 
 PMID:25729585
                                    
                                
                                    Reasoning over taxonomic change: exploring alignments for the Perelleschus use case. 
 PMID:25700173
                                    
                                
                                    Aber-OWL: a framework for ontology-based data access in biology. 
 PMID:25627673
                                    
                                
                                    EXACT2: the semantics of biomedical protocols. 
 PMID:25472549
                                    
                                
                                    An ontology for microbial phenotypes. 
 PMID:25433798
                                    
                                
                                    Annotation of phenotypic diversity: decoupling data curation and ontology curation using Phenex. 
 PMID:25411634
                                    
                                
                                    iBeetle-Base: a database for RNAi phenotypes in the red flour beetle Tribolium castaneum. 
 PMID:25378303
                                    
                                
                                    Organ system heterogeneity DB: a database for the visualization of phenotypes at the organ system level. 
 PMID:25313158
                                    
                                
                                    Molecularly and clinically related drugs and diseases are enriched in phenotypically similar drug-disease pairs. 
 PMID:25276232
                                    
                                
                                    Nose to tail, roots to shoots: spatial descriptors for phenotypic diversity in the Biological Spatial Ontology. 
 PMID:25140222
                                    
                                
                                    The influence of disease categories on gene candidate predictions from model organism phenotypes. 
 PMID:25093073
                                    
                                
                                    The Software Ontology (SWO): a resource for reproducibility in biomedical data analysis, curation and digital preservation. 
 PMID:25068035
                                    
                                
                                    Standardized description of scientific evidence using the Evidence Ontology (ECO). 
 PMID:25052702
                                    
                                
                                    Phenotype ontologies and cross-species analysis for translational research. 
 PMID:24699242
                                    
                                
                                    Linking tissues to phenotypes using gene expression profiles. 
 PMID:24634472
                                    
                                
                                    Semantic integration of gene expression analysis tools and data sources using software connectors. 
 PMID:24341380
                                    
                                
                                    RARGE II: an integrated phenotype database of Arabidopsis mutant traits using a controlled vocabulary. 
 PMID:24272250
                                    
                                
                                    Analyzing gene expression data in mice with the Neuro Behavior Ontology. 
 PMID:24177753
                                    
                                
                                    Improved exome prioritization of disease genes through cross-species phenotype comparison. 
 PMID:24162188
                                    
                                
                                    Mouse model phenotypes provide information about human drug targets. 
 PMID:24158600
                                    
                                
                                    Automatically transforming pre- to post-composed phenotypes: EQ-lising HPO and MP. 
 PMID:24131519
                                    
                                
                                    The ontology of craniofacial development and malformation for translational craniofacial research. 
 PMID:24124010
                                    
                                
                                    Using ontologies to study cell transitions. 
 PMID:24103098
                                    
                                
                                    The Gene Ontology (GO) Cellular Component Ontology: integration with SAO (Subcellular Anatomy Ontology) and other recent developments. 
 PMID:24093723
                                    
                                
                                    Toward knowledge support for analysis and interpretation of complex traits. 
 PMID:24079802
                                    
                                
                                    Manteia, a predictive data mining system for vertebrate genes and its applications to human genetic diseases. 
 PMID:24038354
                                    
                                
                                    The mouse pathology ontology, MPATH; structure and applications. 
 PMID:24033988
                                    
                                
                                    TrOn: an anatomical ontology for the beetle Tribolium castaneum. 
 PMID:23936240
                                    
                                
                                    An integrative, translational approach to understanding rare and orphan genetically based diseases. 
 PMID:23853703
                                    
                                
                                    A knowledge based approach to matching human neurodegenerative disease and animal models. 
 PMID:23717278
                                    
                                
                                    Modeling functional Magnetic Resonance Imaging (fMRI) experimental variables in the Ontology of Experimental Variables and Values (OoEVV). 
 PMID:23684873
                                    
                                
                                    PhenoDigm: analyzing curated annotations to associate animal models with human diseases. 
 PMID:23660285
                                    
                                
                                    FYPO: the fission yeast phenotype ontology. 
 PMID:23658422
                                    
                                
                                    A semantic model for species description applied to the ensign wasps (hymenoptera: evaniidae) of New Caledonia. 
 PMID:23652347
                                    
                                
                                    Systematic analysis of experimental phenotype data reveals gene functions. 
 PMID:23626672
                                    
                                
                                    Decomposing phenotype descriptions for the human skeletal phenome. 
 PMID:23440304
                                    
                                
                                    Towards a bioinformatics of patterning: a computational approach to understanding regulative morphogenesis. 
 PMID:23429669
                                    
                                
                                    A unified anatomy ontology of the vertebrate skeletal system. 
 PMID:23251424
                                    
                                
                                    Semantically enabling a genome-wide association study database. 
 PMID:23244533
                                    
                                
                                    H2DB: a heritability database across multiple species by annotating trait-associated genomic loci. 
 PMID:23193255
                                    
                                
                                    A revision of Evaniscus (Hymenoptera, Evaniidae) using ontology-based semantic phenotype annotation. 
 PMID:23166458
                                    
                                
                                    DcGO: database of domain-centric ontologies on functions, phenotypes, diseases and more. 
 PMID:23161684
                                    
                                
                                    Phenotypic overlap in the contribution of individual genes to CNV pathogenicity revealed by cross-species computational analysis of single-gene mutations in humans, mice and zebrafish. 
 PMID:23104991
                                    
                                
                                    A UML profile for the OBO relation ontology. 
 PMID:23095840
                                    
                                
                                    ZFIN, the Zebrafish Model Organism Database: increased support for mutants and transgenics. 
 PMID:23074187
                                    
                                
                                    Cross-Ontology multi-level association rule mining in the Gene Ontology. 
 PMID:23071802
                                    
                                
                                    Continuation-like semantics for modeling structural process anomalies. 
 PMID:23046705
                                    
                                
                                    Ontology-based cross-species integration and analysis of Saccharomyces cerevisiae phenotypes. 
 PMID:23046642
                                    
                                
                                    Towards improving phenotype representation in OWL. 
 PMID:23046625
                                    
                                
                                    Open biomedical pluralism: formalising knowledge about breast cancer phenotypes. 
 PMID:23046572
                                    
                                
                                    Quantitative comparison of mapping methods between Human and Mammalian Phenotype Ontology. 
 PMID:23046555
                                    
                                
                                    Evaluation of research in biomedical ontologies. 
 PMID:22962340
                                    
                                
                                    The Mammalian Phenotype Ontology as a unifying standard for experimental and high-throughput phenotyping data. 
 PMID:22961259
                                    
                                
                                    Querying phenotype-genotype relationships on patient datasets using semantic web technology: the example of Cerebrotendinous xanthomatosis. 
 PMID:22849591
                                    
                                
                                    Ontologies as integrative tools for plant science. 
 PMID:22847540
                                    
                                
                                    Computational tools for comparative phenomics: the role and promise of ontologies. 
 PMID:22814867
                                    
                                
                                    Improving disease gene prioritization by comparing the semantic similarity of phenotypes in mice with those of human diseases. 
 PMID:22719993
                                    
                                
                                    Three ontologies to define phenotype measurement data. 
 PMID:22654893
                                    
                                
                                    Semantic integration of physiology phenotypes with an application to the Cellular Phenotype Ontology. 
 PMID:22539675
                                    
                                
                                    NeXML: rich, extensible, and verifiable representation of comparative data and metadata. 
 PMID:22357728
                                    
                                
                                    MouseFinder: Candidate disease genes from mouse phenotype data. 
 PMID:22331800
                                    
                                
                                    Uberon, an integrative multi-species anatomy ontology. 
 PMID:22293552
                                    
                                
                                    Disease Ontology: a backbone for disease semantic integration. 
 PMID:22080554
                                    
                                
                                    Improving ontologies by automatic reasoning and evaluation of logical definitions. 
 PMID:22032770
                                    
                                
                                    OBML - Ontologies in Biomedicine and Life Sciences. 
 PMID:21996496
                                    
                                
                                    New approaches to the representation and analysis of phenotype knowledge in human diseases and their animal models. 
 PMID:21987712
                                    
                                
                                    Integrating systems biology models and biomedical ontologies. 
 PMID:21835028
                                    
                                
                                    Interoperability between biomedical ontologies through relation expansion, upper-level ontologies and automatic reasoning. 
 PMID:21789201
                                    
                                
                                    PhenomeNET: a whole-phenome approach to disease gene discovery. 
 PMID:21737429
                                    
                                
                                    Computable visually observed phenotype ontological framework for plants. 
 PMID:21702966
                                    
                                
                                    The cognitive paradigm ontology: design and application. 
 PMID:21643732
                                    
                                
                                    Developing a kidney and urinary pathway knowledge base. 
 PMID:21624162
                                    
                                
                                    PHENOPSIS DB: an information system for Arabidopsis thaliana phenotypic data in an environmental context. 
 PMID:21554668
                                    
                                
                                    A common layer of interoperability for biomedical ontologies based on OWL EL. 
 PMID:21343142
                                    
                                
                                    Worm Phenotype Ontology: integrating phenotype data within and beyond the C. elegans community. 
 PMID:21261995
                                    
                                
                                    Trends in computational biology—2010. 
 PMID:21221103
                                    
                                
                                    The RIKEN integrated database of mammals. 
 PMID:21076152
                                    
                                
                                    Laboratory mouse models for the human genome-wide associations. 
 PMID:21072174
                                    
                                
                                    Interoperability between phenotype and anatomy ontologies. 
 PMID:20971987
                                    
                                
                                    ParameciumDB in 2011: new tools and new data for functional and comparative genomics of the model ciliate Paramecium tetraurelia. 
 PMID:20952411
                                    
                                
                                    Applying the functional abnormality ontology pattern to anatomical functions. 
 PMID:20618982
                                    
                                
                                    The teleost anatomy ontology: anatomical representation for the genomics age. 
 PMID:20547776
                                    
                                
                                    Evolutionary characters, phenotypes and ontologies: curating data from the systematic biology literature. 
 PMID:20505755
                                    
                                
                                    Phenex: ontological annotation of phenotypic diversity. 
 PMID:20463926
                                    
                                
                                    Phenotype ontologies for mouse and man: bridging the semantic gap. 
 PMID:20427557
                                    
                                
                                    Cross-product extensions of the Gene Ontology. 
 PMID:20152934
                                    
                                
                                    Hematopoietic cell types: prototype for a revised cell ontology. 
 PMID:20123131
                                    
                                
                                    Linking human diseases to animal models using ontology-based phenotype annotation. 
 PMID:19956802