Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP682240.RAaLBGXwD-FfGOibUCsA9zYs-vX8giE_R5IEt_6ouHFes130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP682240.RAaLBGXwD-FfGOibUCsA9zYs-vX8giE_R5IEt_6ouHFes130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682240.RAaLBGXwD-FfGOibUCsA9zYs-vX8giE_R5IEt_6ouHFes130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682240.RAaLBGXwD-FfGOibUCsA9zYs-vX8giE_R5IEt_6ouHFes130_provenance.
- NP682240.RAaLBGXwD-FfGOibUCsA9zYs-vX8giE_R5IEt_6ouHFes130_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." NP682240.RAaLBGXwD-FfGOibUCsA9zYs-vX8giE_R5IEt_6ouHFes130_provenance.
- NP682240.RAaLBGXwD-FfGOibUCsA9zYs-vX8giE_R5IEt_6ouHFes130_assertion evidence source_evidence_literature NP682240.RAaLBGXwD-FfGOibUCsA9zYs-vX8giE_R5IEt_6ouHFes130_provenance.
- NP682240.RAaLBGXwD-FfGOibUCsA9zYs-vX8giE_R5IEt_6ouHFes130_assertion SIO_000772 21430528 NP682240.RAaLBGXwD-FfGOibUCsA9zYs-vX8giE_R5IEt_6ouHFes130_provenance.
- NP682240.RAaLBGXwD-FfGOibUCsA9zYs-vX8giE_R5IEt_6ouHFes130_assertion wasDerivedFrom befree-20150227 NP682240.RAaLBGXwD-FfGOibUCsA9zYs-vX8giE_R5IEt_6ouHFes130_provenance.
- NP682240.RAaLBGXwD-FfGOibUCsA9zYs-vX8giE_R5IEt_6ouHFes130_assertion wasGeneratedBy ECO_0000203 NP682240.RAaLBGXwD-FfGOibUCsA9zYs-vX8giE_R5IEt_6ouHFes130_provenance.
- befree-20150227 importedOn "2015-02-27" NP682240.RAaLBGXwD-FfGOibUCsA9zYs-vX8giE_R5IEt_6ouHFes130_provenance.