Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP134528.RAQANuxEU0A9RjNEwMR7YiPBtYxZ5la4RwHK0etk8juGk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP134528.RAQANuxEU0A9RjNEwMR7YiPBtYxZ5la4RwHK0etk8juGk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP134528.RAQANuxEU0A9RjNEwMR7YiPBtYxZ5la4RwHK0etk8juGk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP134528.RAQANuxEU0A9RjNEwMR7YiPBtYxZ5la4RwHK0etk8juGk130_provenance.
- NP134528.RAQANuxEU0A9RjNEwMR7YiPBtYxZ5la4RwHK0etk8juGk130_assertion description "[loss-of-function mutations in genes encoding the cardiac L-type calcium channel to be associated with a familial sudden cardiac death syndrome in which a Brugada syndrome phenotype is combined with shorter-than-normal QT intervals ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP134528.RAQANuxEU0A9RjNEwMR7YiPBtYxZ5la4RwHK0etk8juGk130_provenance.
- NP134528.RAQANuxEU0A9RjNEwMR7YiPBtYxZ5la4RwHK0etk8juGk130_assertion evidence source_evidence_literature NP134528.RAQANuxEU0A9RjNEwMR7YiPBtYxZ5la4RwHK0etk8juGk130_provenance.
- NP134528.RAQANuxEU0A9RjNEwMR7YiPBtYxZ5la4RwHK0etk8juGk130_assertion SIO_000772 17224476 NP134528.RAQANuxEU0A9RjNEwMR7YiPBtYxZ5la4RwHK0etk8juGk130_provenance.
- NP134528.RAQANuxEU0A9RjNEwMR7YiPBtYxZ5la4RwHK0etk8juGk130_assertion wasDerivedFrom lhgdn-20090331 NP134528.RAQANuxEU0A9RjNEwMR7YiPBtYxZ5la4RwHK0etk8juGk130_provenance.
- NP134528.RAQANuxEU0A9RjNEwMR7YiPBtYxZ5la4RwHK0etk8juGk130_assertion wasGeneratedBy ECO_0000203 NP134528.RAQANuxEU0A9RjNEwMR7YiPBtYxZ5la4RwHK0etk8juGk130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP134528.RAQANuxEU0A9RjNEwMR7YiPBtYxZ5la4RwHK0etk8juGk130_provenance.