Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP446739.RAJHAZsRemrrKKEFhvw9CwcpBzQZP1Eqvf5OgCqQVC-og130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP446739.RAJHAZsRemrrKKEFhvw9CwcpBzQZP1Eqvf5OgCqQVC-og130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP446739.RAJHAZsRemrrKKEFhvw9CwcpBzQZP1Eqvf5OgCqQVC-og130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP446739.RAJHAZsRemrrKKEFhvw9CwcpBzQZP1Eqvf5OgCqQVC-og130_provenance.
- NP446739.RAJHAZsRemrrKKEFhvw9CwcpBzQZP1Eqvf5OgCqQVC-og130_assertion description "[A decrease of IKr or IKs by mutations in either HERG, KvLQT1, or KCNE family results in inherited long QT syndrome (LQTS) with high risk for Torsades de pointes (TdP)-type polymorphic ventricular tachycardia and ventricular fibrillation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP446739.RAJHAZsRemrrKKEFhvw9CwcpBzQZP1Eqvf5OgCqQVC-og130_provenance.
- NP446739.RAJHAZsRemrrKKEFhvw9CwcpBzQZP1Eqvf5OgCqQVC-og130_assertion evidence source_evidence_literature NP446739.RAJHAZsRemrrKKEFhvw9CwcpBzQZP1Eqvf5OgCqQVC-og130_provenance.
- NP446739.RAJHAZsRemrrKKEFhvw9CwcpBzQZP1Eqvf5OgCqQVC-og130_assertion SIO_000772 14769199 NP446739.RAJHAZsRemrrKKEFhvw9CwcpBzQZP1Eqvf5OgCqQVC-og130_provenance.
- NP446739.RAJHAZsRemrrKKEFhvw9CwcpBzQZP1Eqvf5OgCqQVC-og130_assertion wasDerivedFrom befree-20140225 NP446739.RAJHAZsRemrrKKEFhvw9CwcpBzQZP1Eqvf5OgCqQVC-og130_provenance.
- NP446739.RAJHAZsRemrrKKEFhvw9CwcpBzQZP1Eqvf5OgCqQVC-og130_assertion wasGeneratedBy ECO_0000203 NP446739.RAJHAZsRemrrKKEFhvw9CwcpBzQZP1Eqvf5OgCqQVC-og130_provenance.
- befree-20140225 importedOn "2014-02-25" NP446739.RAJHAZsRemrrKKEFhvw9CwcpBzQZP1Eqvf5OgCqQVC-og130_provenance.