Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP723774.RAf2REXZuhkJJ87nlQ2p2zlpSEmjn_ljoImSv6Oenh_nA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP723774.RAf2REXZuhkJJ87nlQ2p2zlpSEmjn_ljoImSv6Oenh_nA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP723774.RAf2REXZuhkJJ87nlQ2p2zlpSEmjn_ljoImSv6Oenh_nA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP723774.RAf2REXZuhkJJ87nlQ2p2zlpSEmjn_ljoImSv6Oenh_nA130_provenance.
- NP723774.RAf2REXZuhkJJ87nlQ2p2zlpSEmjn_ljoImSv6Oenh_nA130_assertion description "[Mutations of GNAT1 and GNAT2, which encode the retinal G proteins (transducins), are rare causes of specific congenital visual defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723774.RAf2REXZuhkJJ87nlQ2p2zlpSEmjn_ljoImSv6Oenh_nA130_provenance.
- NP723774.RAf2REXZuhkJJ87nlQ2p2zlpSEmjn_ljoImSv6Oenh_nA130_assertion evidence source_evidence_literature NP723774.RAf2REXZuhkJJ87nlQ2p2zlpSEmjn_ljoImSv6Oenh_nA130_provenance.
- NP723774.RAf2REXZuhkJJ87nlQ2p2zlpSEmjn_ljoImSv6Oenh_nA130_assertion SIO_000772 16600389 NP723774.RAf2REXZuhkJJ87nlQ2p2zlpSEmjn_ljoImSv6Oenh_nA130_provenance.
- NP723774.RAf2REXZuhkJJ87nlQ2p2zlpSEmjn_ljoImSv6Oenh_nA130_assertion wasDerivedFrom befree-20140225 NP723774.RAf2REXZuhkJJ87nlQ2p2zlpSEmjn_ljoImSv6Oenh_nA130_provenance.
- NP723774.RAf2REXZuhkJJ87nlQ2p2zlpSEmjn_ljoImSv6Oenh_nA130_assertion wasGeneratedBy ECO_0000203 NP723774.RAf2REXZuhkJJ87nlQ2p2zlpSEmjn_ljoImSv6Oenh_nA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP723774.RAf2REXZuhkJJ87nlQ2p2zlpSEmjn_ljoImSv6Oenh_nA130_provenance.