Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP430932.RAmIbtyvJoA2G1IhlQzS26k9zXCOlQkOEepLUX5VIn2PE130_assertion> ?p ?o ?g. }
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- NP430932.RAmIbtyvJoA2G1IhlQzS26k9zXCOlQkOEepLUX5VIn2PE130_assertion type Assertion NP430932.RAmIbtyvJoA2G1IhlQzS26k9zXCOlQkOEepLUX5VIn2PE130_head.
- NP430932.RAmIbtyvJoA2G1IhlQzS26k9zXCOlQkOEepLUX5VIn2PE130_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." NP430932.RAmIbtyvJoA2G1IhlQzS26k9zXCOlQkOEepLUX5VIn2PE130_provenance.
- NP430932.RAmIbtyvJoA2G1IhlQzS26k9zXCOlQkOEepLUX5VIn2PE130_assertion evidence source_evidence_literature NP430932.RAmIbtyvJoA2G1IhlQzS26k9zXCOlQkOEepLUX5VIn2PE130_provenance.
- NP430932.RAmIbtyvJoA2G1IhlQzS26k9zXCOlQkOEepLUX5VIn2PE130_assertion SIO_000772 14769199 NP430932.RAmIbtyvJoA2G1IhlQzS26k9zXCOlQkOEepLUX5VIn2PE130_provenance.
- NP430932.RAmIbtyvJoA2G1IhlQzS26k9zXCOlQkOEepLUX5VIn2PE130_assertion wasDerivedFrom befree-2016 NP430932.RAmIbtyvJoA2G1IhlQzS26k9zXCOlQkOEepLUX5VIn2PE130_provenance.
- NP430932.RAmIbtyvJoA2G1IhlQzS26k9zXCOlQkOEepLUX5VIn2PE130_assertion wasGeneratedBy ECO_0000203 NP430932.RAmIbtyvJoA2G1IhlQzS26k9zXCOlQkOEepLUX5VIn2PE130_provenance.