Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP674259.RAavhnVGYidcpPu6u_P2un4Y0y2VOTQrURYsTH5snnpkI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP674259.RAavhnVGYidcpPu6u_P2un4Y0y2VOTQrURYsTH5snnpkI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP674259.RAavhnVGYidcpPu6u_P2un4Y0y2VOTQrURYsTH5snnpkI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP674259.RAavhnVGYidcpPu6u_P2un4Y0y2VOTQrURYsTH5snnpkI130_provenance.
- NP674259.RAavhnVGYidcpPu6u_P2un4Y0y2VOTQrURYsTH5snnpkI130_assertion description "[Autosomal recessive Robinow syndrome (OMIM 268310) is a condition caused by mutations in the ROR2 gene, the receptor tyrosine kinase-like orphan receptor 2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674259.RAavhnVGYidcpPu6u_P2un4Y0y2VOTQrURYsTH5snnpkI130_provenance.
- NP674259.RAavhnVGYidcpPu6u_P2un4Y0y2VOTQrURYsTH5snnpkI130_assertion evidence source_evidence_literature NP674259.RAavhnVGYidcpPu6u_P2un4Y0y2VOTQrURYsTH5snnpkI130_provenance.
- NP674259.RAavhnVGYidcpPu6u_P2un4Y0y2VOTQrURYsTH5snnpkI130_assertion SIO_000772 22178368 NP674259.RAavhnVGYidcpPu6u_P2un4Y0y2VOTQrURYsTH5snnpkI130_provenance.
- NP674259.RAavhnVGYidcpPu6u_P2un4Y0y2VOTQrURYsTH5snnpkI130_assertion wasDerivedFrom befree-20150227 NP674259.RAavhnVGYidcpPu6u_P2un4Y0y2VOTQrURYsTH5snnpkI130_provenance.
- NP674259.RAavhnVGYidcpPu6u_P2un4Y0y2VOTQrURYsTH5snnpkI130_assertion wasGeneratedBy ECO_0000203 NP674259.RAavhnVGYidcpPu6u_P2un4Y0y2VOTQrURYsTH5snnpkI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP674259.RAavhnVGYidcpPu6u_P2un4Y0y2VOTQrURYsTH5snnpkI130_provenance.