PhenoMiner
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Database of phenotypes extracted from the scientific literature using text mining.
Description
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Database of phenotypes extracted from the scientific literature using text mining.
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:32:23.960344
Webpage:
http://phenominer.mml.cam.ac.uk/Webpage
More detailed information about this field from each metasource.
http://phenominer.mml.cam.ac.uk/
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:32:23.960344
Publications:
Publications
More detailed information about this field from each metasource.
PhenoMiner: from text to a database of phenotypes associated with OMIM diseases
PMID: 26507285
metasource: bio.tools
version: extracted_at: 2022-11-04T11:32:23.960344
Publications
More detailed information about this field from each metasource.
PhenoMiner: from text to a database of phenotypes associated with OMIM diseases
PMID: 26507285
metasource: bio.tools
version: extracted_at: 2022-11-04T11:32:23.960344
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PhenoMiner: from text to a database of phenotypes associated with OMIM diseases
PubMed citations: 13.
13 articles citing: PhenoMiner: from text to a database of phenotypes associated with OMIM diseases
DeepPheno: Predicting single gene loss-of-function phenotypes using an ontology-aware hierarchical classifier. PMID:33206638
Recent advances in biomedical literature mining. PMID:32422651
Automated Methods Enable Direct Computation on Phenotypic Descriptions for Novel Candidate Gene Prediction. PMID:31998331
Annotating and detecting phenotypic information for chronic obstructive pulmonary disease. PMID:31984360
Applying citizen science to gene, drug and disease relationship extraction from biomedical abstracts. PMID:31504205
The utility of phenomics in diagnosis of inherited metabolic disorders. PMID:30651242
Genetics of Human Primary Hypertension: Focus on Hormonal Mechanisms. PMID:30590482
A gene-phenotype relationship extraction pipeline from the biomedical literature using a representation learning approach. PMID:29950017
TiSAn: estimating tissue-specific effects of coding and non-coding variants. PMID:29912365
Phenotype Instance Verification and Evaluation Tool (PIVET): A Scaled Phenotype Evidence Generation Framework Using Web-Based Medical Literature. PMID:29728351
A new synonym-substitution method to enrich the human phenotype ontology. PMID:29017443
NiaoDuQing granules relieve chronic kidney disease symptoms by decreasing renal fibrosis and anemia. PMID:28915563
Novel bioinformatic developments for exome sequencing. PMID:27075447
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