Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP365873.RA_bnlzu76DLE6sS-xmTKjX3QYx1Osr5RoyAu3xPnts6s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP365873.RA_bnlzu76DLE6sS-xmTKjX3QYx1Osr5RoyAu3xPnts6s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP365873.RA_bnlzu76DLE6sS-xmTKjX3QYx1Osr5RoyAu3xPnts6s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP365873.RA_bnlzu76DLE6sS-xmTKjX3QYx1Osr5RoyAu3xPnts6s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP365873.RA_bnlzu76DLE6sS-xmTKjX3QYx1Osr5RoyAu3xPnts6s130_provenance.
- NP365873.RA_bnlzu76DLE6sS-xmTKjX3QYx1Osr5RoyAu3xPnts6s130_assertion wasGeneratedBy ECO_0000203 NP365873.RA_bnlzu76DLE6sS-xmTKjX3QYx1Osr5RoyAu3xPnts6s130_provenance.
- NP365873.RA_bnlzu76DLE6sS-xmTKjX3QYx1Osr5RoyAu3xPnts6s130_assertion wasDerivedFrom befree-20150227 NP365873.RA_bnlzu76DLE6sS-xmTKjX3QYx1Osr5RoyAu3xPnts6s130_provenance.
- NP365873.RA_bnlzu76DLE6sS-xmTKjX3QYx1Osr5RoyAu3xPnts6s130_assertion SIO_000772 10942418 NP365873.RA_bnlzu76DLE6sS-xmTKjX3QYx1Osr5RoyAu3xPnts6s130_provenance.
- NP365873.RA_bnlzu76DLE6sS-xmTKjX3QYx1Osr5RoyAu3xPnts6s130_assertion evidence source_evidence_literature NP365873.RA_bnlzu76DLE6sS-xmTKjX3QYx1Osr5RoyAu3xPnts6s130_provenance.
- NP365873.RA_bnlzu76DLE6sS-xmTKjX3QYx1Osr5RoyAu3xPnts6s130_assertion description "[The WS4 phenotype can result from mutations in the endothelin-B receptor gene (EDNRB), in the gene for its ligand, endothelin-3 (EDN3), or in the SOX10 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP365873.RA_bnlzu76DLE6sS-xmTKjX3QYx1Osr5RoyAu3xPnts6s130_provenance.