Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP430935.RAjg_aw5MjK68H8FjRtZH0EPXtlE9byC2pYJAK-wNy-EE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP430935.RAjg_aw5MjK68H8FjRtZH0EPXtlE9byC2pYJAK-wNy-EE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP430935.RAjg_aw5MjK68H8FjRtZH0EPXtlE9byC2pYJAK-wNy-EE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP430935.RAjg_aw5MjK68H8FjRtZH0EPXtlE9byC2pYJAK-wNy-EE130_provenance.
- NP430935.RAjg_aw5MjK68H8FjRtZH0EPXtlE9byC2pYJAK-wNy-EE130_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." NP430935.RAjg_aw5MjK68H8FjRtZH0EPXtlE9byC2pYJAK-wNy-EE130_provenance.
- NP430935.RAjg_aw5MjK68H8FjRtZH0EPXtlE9byC2pYJAK-wNy-EE130_assertion evidence source_evidence_literature NP430935.RAjg_aw5MjK68H8FjRtZH0EPXtlE9byC2pYJAK-wNy-EE130_provenance.
- NP430935.RAjg_aw5MjK68H8FjRtZH0EPXtlE9byC2pYJAK-wNy-EE130_assertion SIO_000772 14769199 NP430935.RAjg_aw5MjK68H8FjRtZH0EPXtlE9byC2pYJAK-wNy-EE130_provenance.
- NP430935.RAjg_aw5MjK68H8FjRtZH0EPXtlE9byC2pYJAK-wNy-EE130_assertion wasDerivedFrom befree-2016 NP430935.RAjg_aw5MjK68H8FjRtZH0EPXtlE9byC2pYJAK-wNy-EE130_provenance.
- NP430935.RAjg_aw5MjK68H8FjRtZH0EPXtlE9byC2pYJAK-wNy-EE130_assertion wasGeneratedBy ECO_0000203 NP430935.RAjg_aw5MjK68H8FjRtZH0EPXtlE9byC2pYJAK-wNy-EE130_provenance.
- befree-2016 importedOn "2016-02-19" NP430935.RAjg_aw5MjK68H8FjRtZH0EPXtlE9byC2pYJAK-wNy-EE130_provenance.