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PhenoMiner: from text to a database of phenotypes associated with OMIM diseases
Analysis of scientific and clinical phenotypes reported in the experimental literature has been curated manually to build high-quality databases such as the Online Mendelian Inheritance in Man (OMIM). However, the identification and harmonization of phenotype descriptions struggles with the diversit...
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| Publicado no: | Database (Oxford) |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4622021/ https://ncbi.nlm.nih.gov/pubmed/26507285 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/database/bav104 |
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