Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP523250.RAOYE738BHCtaWP_Vp0xo7B1qk4TJ1DCbZPMY_120EIqE130_assertion> ?p ?o ?g. }
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- NP523250.RAOYE738BHCtaWP_Vp0xo7B1qk4TJ1DCbZPMY_120EIqE130_assertion type Assertion NP523250.RAOYE738BHCtaWP_Vp0xo7B1qk4TJ1DCbZPMY_120EIqE130_head.
- 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.