Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP881817.RAgBTxHhIUrlz9azDVsZjTD_ujDzaI5av4zy1D965gz_I130_assertion> ?p ?o ?g. }
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- NP881817.RAgBTxHhIUrlz9azDVsZjTD_ujDzaI5av4zy1D965gz_I130_assertion type Assertion NP881817.RAgBTxHhIUrlz9azDVsZjTD_ujDzaI5av4zy1D965gz_I130_head.
- NP881817.RAgBTxHhIUrlz9azDVsZjTD_ujDzaI5av4zy1D965gz_I130_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." NP881817.RAgBTxHhIUrlz9azDVsZjTD_ujDzaI5av4zy1D965gz_I130_provenance.
- NP881817.RAgBTxHhIUrlz9azDVsZjTD_ujDzaI5av4zy1D965gz_I130_assertion evidence source_evidence_literature NP881817.RAgBTxHhIUrlz9azDVsZjTD_ujDzaI5av4zy1D965gz_I130_provenance.
- NP881817.RAgBTxHhIUrlz9azDVsZjTD_ujDzaI5av4zy1D965gz_I130_assertion SIO_000772 21430528 NP881817.RAgBTxHhIUrlz9azDVsZjTD_ujDzaI5av4zy1D965gz_I130_provenance.
- NP881817.RAgBTxHhIUrlz9azDVsZjTD_ujDzaI5av4zy1D965gz_I130_assertion wasDerivedFrom befree-2016 NP881817.RAgBTxHhIUrlz9azDVsZjTD_ujDzaI5av4zy1D965gz_I130_provenance.
- NP881817.RAgBTxHhIUrlz9azDVsZjTD_ujDzaI5av4zy1D965gz_I130_assertion wasGeneratedBy ECO_0000203 NP881817.RAgBTxHhIUrlz9azDVsZjTD_ujDzaI5av4zy1D965gz_I130_provenance.