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- NP705747.RACeg_8i1whA8htiq8lc3uYQ9i-YA5sdD6ghkq9SgQ0S8130_assertion type Assertion NP705747.RACeg_8i1whA8htiq8lc3uYQ9i-YA5sdD6ghkq9SgQ0S8130_head.
- NP705747.RACeg_8i1whA8htiq8lc3uYQ9i-YA5sdD6ghkq9SgQ0S8130_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." NP705747.RACeg_8i1whA8htiq8lc3uYQ9i-YA5sdD6ghkq9SgQ0S8130_provenance.
- NP705747.RACeg_8i1whA8htiq8lc3uYQ9i-YA5sdD6ghkq9SgQ0S8130_assertion evidence source_evidence_literature NP705747.RACeg_8i1whA8htiq8lc3uYQ9i-YA5sdD6ghkq9SgQ0S8130_provenance.
- NP705747.RACeg_8i1whA8htiq8lc3uYQ9i-YA5sdD6ghkq9SgQ0S8130_assertion SIO_000772 21430528 NP705747.RACeg_8i1whA8htiq8lc3uYQ9i-YA5sdD6ghkq9SgQ0S8130_provenance.
- NP705747.RACeg_8i1whA8htiq8lc3uYQ9i-YA5sdD6ghkq9SgQ0S8130_assertion wasDerivedFrom befree-20150227 NP705747.RACeg_8i1whA8htiq8lc3uYQ9i-YA5sdD6ghkq9SgQ0S8130_provenance.
- NP705747.RACeg_8i1whA8htiq8lc3uYQ9i-YA5sdD6ghkq9SgQ0S8130_assertion wasGeneratedBy ECO_0000203 NP705747.RACeg_8i1whA8htiq8lc3uYQ9i-YA5sdD6ghkq9SgQ0S8130_provenance.