Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP881817.RAgBTxHhIUrlz9azDVsZjTD_ujDzaI5av4zy1D965gz_I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP881817.RAgBTxHhIUrlz9azDVsZjTD_ujDzaI5av4zy1D965gz_I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP881817.RAgBTxHhIUrlz9azDVsZjTD_ujDzaI5av4zy1D965gz_I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP881817.RAgBTxHhIUrlz9azDVsZjTD_ujDzaI5av4zy1D965gz_I130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP881817.RAgBTxHhIUrlz9azDVsZjTD_ujDzaI5av4zy1D965gz_I130_provenance.