Bio2RDF::OMIM

OMIM is a comprehensive, authoritative, and timely compendium of human genes and genetic phenotypes. The full-text, referenced overviews in OMIM contain information on all known mendelian disorders and over 12,000 genes. OMIM focuses on the relationship between phenotype and genotype.

Data and Resources

Additional Info

Fält Värde
Källa http://omim.bio2rdf.org
Skapare Bio2RDF
Förvaltare Michel Dumontier
namespace http://bio2rdf.org/omim:

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