Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP488144.RAOxlOnYJPVlgVlGMe8trk3j6XKETjnxD350i8_AEWeYE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP488144.RAOxlOnYJPVlgVlGMe8trk3j6XKETjnxD350i8_AEWeYE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP488144.RAOxlOnYJPVlgVlGMe8trk3j6XKETjnxD350i8_AEWeYE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP488144.RAOxlOnYJPVlgVlGMe8trk3j6XKETjnxD350i8_AEWeYE130_provenance.
- NP488144.RAOxlOnYJPVlgVlGMe8trk3j6XKETjnxD350i8_AEWeYE130_assertion description "[Loss of function mutations in SCN5A, encoding the cardiac sodium channel, are one cause of the Brugada syndrome, associated with slow conduction and a high incidence of ventricular fibrillation, especially in Asians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP488144.RAOxlOnYJPVlgVlGMe8trk3j6XKETjnxD350i8_AEWeYE130_provenance.
- NP488144.RAOxlOnYJPVlgVlGMe8trk3j6XKETjnxD350i8_AEWeYE130_assertion evidence source_evidence_literature NP488144.RAOxlOnYJPVlgVlGMe8trk3j6XKETjnxD350i8_AEWeYE130_provenance.
- NP488144.RAOxlOnYJPVlgVlGMe8trk3j6XKETjnxD350i8_AEWeYE130_assertion SIO_000772 16415376 NP488144.RAOxlOnYJPVlgVlGMe8trk3j6XKETjnxD350i8_AEWeYE130_provenance.
- NP488144.RAOxlOnYJPVlgVlGMe8trk3j6XKETjnxD350i8_AEWeYE130_assertion wasDerivedFrom befree-20140225 NP488144.RAOxlOnYJPVlgVlGMe8trk3j6XKETjnxD350i8_AEWeYE130_provenance.
- NP488144.RAOxlOnYJPVlgVlGMe8trk3j6XKETjnxD350i8_AEWeYE130_assertion wasGeneratedBy ECO_0000203 NP488144.RAOxlOnYJPVlgVlGMe8trk3j6XKETjnxD350i8_AEWeYE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP488144.RAOxlOnYJPVlgVlGMe8trk3j6XKETjnxD350i8_AEWeYE130_provenance.