Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP523250.RAOYE738BHCtaWP_Vp0xo7B1qk4TJ1DCbZPMY_120EIqE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP523250.RAOYE738BHCtaWP_Vp0xo7B1qk4TJ1DCbZPMY_120EIqE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP523250.RAOYE738BHCtaWP_Vp0xo7B1qk4TJ1DCbZPMY_120EIqE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP523250.RAOYE738BHCtaWP_Vp0xo7B1qk4TJ1DCbZPMY_120EIqE130_provenance.
- NP523250.RAOYE738BHCtaWP_Vp0xo7B1qk4TJ1DCbZPMY_120EIqE130_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." NP523250.RAOYE738BHCtaWP_Vp0xo7B1qk4TJ1DCbZPMY_120EIqE130_provenance.
- NP523250.RAOYE738BHCtaWP_Vp0xo7B1qk4TJ1DCbZPMY_120EIqE130_assertion evidence source_evidence_literature NP523250.RAOYE738BHCtaWP_Vp0xo7B1qk4TJ1DCbZPMY_120EIqE130_provenance.
- NP523250.RAOYE738BHCtaWP_Vp0xo7B1qk4TJ1DCbZPMY_120EIqE130_assertion SIO_000772 14769199 NP523250.RAOYE738BHCtaWP_Vp0xo7B1qk4TJ1DCbZPMY_120EIqE130_provenance.
- NP523250.RAOYE738BHCtaWP_Vp0xo7B1qk4TJ1DCbZPMY_120EIqE130_assertion wasDerivedFrom befree-20150227 NP523250.RAOYE738BHCtaWP_Vp0xo7B1qk4TJ1DCbZPMY_120EIqE130_provenance.
- NP523250.RAOYE738BHCtaWP_Vp0xo7B1qk4TJ1DCbZPMY_120EIqE130_assertion wasGeneratedBy ECO_0000203 NP523250.RAOYE738BHCtaWP_Vp0xo7B1qk4TJ1DCbZPMY_120EIqE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP523250.RAOYE738BHCtaWP_Vp0xo7B1qk4TJ1DCbZPMY_120EIqE130_provenance.