Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP881818.RAtF0c4VFzpuNZdUIQ3B_9ormIIvzsYw75k-PA58O60fE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP881818.RAtF0c4VFzpuNZdUIQ3B_9ormIIvzsYw75k-PA58O60fE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP881818.RAtF0c4VFzpuNZdUIQ3B_9ormIIvzsYw75k-PA58O60fE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP881818.RAtF0c4VFzpuNZdUIQ3B_9ormIIvzsYw75k-PA58O60fE130_provenance.
- NP881818.RAtF0c4VFzpuNZdUIQ3B_9ormIIvzsYw75k-PA58O60fE130_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." NP881818.RAtF0c4VFzpuNZdUIQ3B_9ormIIvzsYw75k-PA58O60fE130_provenance.
- NP881818.RAtF0c4VFzpuNZdUIQ3B_9ormIIvzsYw75k-PA58O60fE130_assertion evidence source_evidence_literature NP881818.RAtF0c4VFzpuNZdUIQ3B_9ormIIvzsYw75k-PA58O60fE130_provenance.
- NP881818.RAtF0c4VFzpuNZdUIQ3B_9ormIIvzsYw75k-PA58O60fE130_assertion SIO_000772 21430528 NP881818.RAtF0c4VFzpuNZdUIQ3B_9ormIIvzsYw75k-PA58O60fE130_provenance.
- NP881818.RAtF0c4VFzpuNZdUIQ3B_9ormIIvzsYw75k-PA58O60fE130_assertion wasDerivedFrom befree-2016 NP881818.RAtF0c4VFzpuNZdUIQ3B_9ormIIvzsYw75k-PA58O60fE130_provenance.
- NP881818.RAtF0c4VFzpuNZdUIQ3B_9ormIIvzsYw75k-PA58O60fE130_assertion wasGeneratedBy ECO_0000203 NP881818.RAtF0c4VFzpuNZdUIQ3B_9ormIIvzsYw75k-PA58O60fE130_provenance.
- befree-2016 importedOn "2016-02-19" NP881818.RAtF0c4VFzpuNZdUIQ3B_9ormIIvzsYw75k-PA58O60fE130_provenance.