Bio2RDFBio2RDFbio2rdfbio2rdfAPI/SPARQLEXAMPLE/RDF+XMLFILEHTMLMETA/VOIDMETA/RDF-SCHEMAMAPPING/OWLMETA/SITEMAPAPPLICATION/X-NQUADSbio2rdfderef-vocabformat-dcformat-rdfformat-rdfslicense-metadatalifescienceslodlodcloud-diagram-2011-09-19lodcloud-diagram-2014-08-30provenance-metadatapublished-by-third-partyvocab-mappingscc-byJul 30, 20162016-07-30
Dataset
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.
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.
Download & API
SPARQL endpointapi/sparql
SPARQL endpoint
Example resource (RDF)example/rdf+xml
Example resource (RDF)
Download page (n-quads, gz compressed)file
Download
Dataset description (HTML)html
Dataset description (HTML)
Dataset description (RDF)meta/void
Dataset description (RDF)
OWL Schemameta/rdf-schema
OWL Schema
Mappings (SIO)mapping/owl
Mappings (SIO)
Semantic Web Sitemapmeta/sitemap
Semantic Web Sitemap
Download (n-quads, gzipped)application/x-nquads
Download omim.nq.gz (n-quads, gzipped)
Sources & license
Sources
License
- cc-by