Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP682210.RAeBoLpNvFA9ENaze_Ny9dNkrvEHiOF2-xL3JUXSEchwA130_assertion> ?p ?o ?g. }
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- NP682210.RAeBoLpNvFA9ENaze_Ny9dNkrvEHiOF2-xL3JUXSEchwA130_assertion type Assertion NP682210.RAeBoLpNvFA9ENaze_Ny9dNkrvEHiOF2-xL3JUXSEchwA130_head.
- NP682210.RAeBoLpNvFA9ENaze_Ny9dNkrvEHiOF2-xL3JUXSEchwA130_assertion description "[In addition to new mutations in known SCD genes, several novel genes not previously implicated in SCD causation have been found, particularly in long QT syndrome (e.g., KCNJ5, AKAP9, SNTA1), idiopathic ventricular fibrillation (e.g., DPP6, KCNJ8), dilated cardiomyopathy (e.g., NEBL), and hypertrophic cardiomyopathy (HCM; e.g., NEXN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682210.RAeBoLpNvFA9ENaze_Ny9dNkrvEHiOF2-xL3JUXSEchwA130_provenance.
- NP682210.RAeBoLpNvFA9ENaze_Ny9dNkrvEHiOF2-xL3JUXSEchwA130_assertion evidence source_evidence_literature NP682210.RAeBoLpNvFA9ENaze_Ny9dNkrvEHiOF2-xL3JUXSEchwA130_provenance.
- NP682210.RAeBoLpNvFA9ENaze_Ny9dNkrvEHiOF2-xL3JUXSEchwA130_assertion SIO_000772 21430528 NP682210.RAeBoLpNvFA9ENaze_Ny9dNkrvEHiOF2-xL3JUXSEchwA130_provenance.
- NP682210.RAeBoLpNvFA9ENaze_Ny9dNkrvEHiOF2-xL3JUXSEchwA130_assertion wasDerivedFrom befree-20150227 NP682210.RAeBoLpNvFA9ENaze_Ny9dNkrvEHiOF2-xL3JUXSEchwA130_provenance.
- NP682210.RAeBoLpNvFA9ENaze_Ny9dNkrvEHiOF2-xL3JUXSEchwA130_assertion wasGeneratedBy ECO_0000203 NP682210.RAeBoLpNvFA9ENaze_Ny9dNkrvEHiOF2-xL3JUXSEchwA130_provenance.