Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP444713.RAKjousVq2Wti2Mbf8G_pzrh4yk6P7kMXhQkLrH96fjNE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP444713.RAKjousVq2Wti2Mbf8G_pzrh4yk6P7kMXhQkLrH96fjNE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP444713.RAKjousVq2Wti2Mbf8G_pzrh4yk6P7kMXhQkLrH96fjNE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP444713.RAKjousVq2Wti2Mbf8G_pzrh4yk6P7kMXhQkLrH96fjNE130_provenance.
- NP444713.RAKjousVq2Wti2Mbf8G_pzrh4yk6P7kMXhQkLrH96fjNE130_assertion description "[Loss-of-function mutations in the gene SCN5A can cause Brugada syndrome (BrS), which is an inherited form of idiopathic ventricular fibrillation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP444713.RAKjousVq2Wti2Mbf8G_pzrh4yk6P7kMXhQkLrH96fjNE130_provenance.
- NP444713.RAKjousVq2Wti2Mbf8G_pzrh4yk6P7kMXhQkLrH96fjNE130_assertion evidence source_evidence_literature NP444713.RAKjousVq2Wti2Mbf8G_pzrh4yk6P7kMXhQkLrH96fjNE130_provenance.
- NP444713.RAKjousVq2Wti2Mbf8G_pzrh4yk6P7kMXhQkLrH96fjNE130_assertion SIO_000772 17897138 NP444713.RAKjousVq2Wti2Mbf8G_pzrh4yk6P7kMXhQkLrH96fjNE130_provenance.
- NP444713.RAKjousVq2Wti2Mbf8G_pzrh4yk6P7kMXhQkLrH96fjNE130_assertion wasDerivedFrom befree-20140225 NP444713.RAKjousVq2Wti2Mbf8G_pzrh4yk6P7kMXhQkLrH96fjNE130_provenance.
- NP444713.RAKjousVq2Wti2Mbf8G_pzrh4yk6P7kMXhQkLrH96fjNE130_assertion wasGeneratedBy ECO_0000203 NP444713.RAKjousVq2Wti2Mbf8G_pzrh4yk6P7kMXhQkLrH96fjNE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP444713.RAKjousVq2Wti2Mbf8G_pzrh4yk6P7kMXhQkLrH96fjNE130_provenance.