Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP661717.RA0zvAxOCEe1t9X-2m__44zIFfBwkpqaa2xFrpB7CnYzI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP661717.RA0zvAxOCEe1t9X-2m__44zIFfBwkpqaa2xFrpB7CnYzI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP661717.RA0zvAxOCEe1t9X-2m__44zIFfBwkpqaa2xFrpB7CnYzI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP661717.RA0zvAxOCEe1t9X-2m__44zIFfBwkpqaa2xFrpB7CnYzI130_provenance.
- NP661717.RA0zvAxOCEe1t9X-2m__44zIFfBwkpqaa2xFrpB7CnYzI130_assertion description "[The existence of SCN5A mutation and clinical variables (syncopal episode, documented ventricular fibrillation [VF], and family history of sudden death) were compared with spontaneous AF episodes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP661717.RA0zvAxOCEe1t9X-2m__44zIFfBwkpqaa2xFrpB7CnYzI130_provenance.
- NP661717.RA0zvAxOCEe1t9X-2m__44zIFfBwkpqaa2xFrpB7CnYzI130_assertion evidence source_evidence_literature NP661717.RA0zvAxOCEe1t9X-2m__44zIFfBwkpqaa2xFrpB7CnYzI130_provenance.
- NP661717.RA0zvAxOCEe1t9X-2m__44zIFfBwkpqaa2xFrpB7CnYzI130_assertion SIO_000772 18355654 NP661717.RA0zvAxOCEe1t9X-2m__44zIFfBwkpqaa2xFrpB7CnYzI130_provenance.
- NP661717.RA0zvAxOCEe1t9X-2m__44zIFfBwkpqaa2xFrpB7CnYzI130_assertion wasDerivedFrom befree-2016 NP661717.RA0zvAxOCEe1t9X-2m__44zIFfBwkpqaa2xFrpB7CnYzI130_provenance.
- NP661717.RA0zvAxOCEe1t9X-2m__44zIFfBwkpqaa2xFrpB7CnYzI130_assertion wasGeneratedBy ECO_0000203 NP661717.RA0zvAxOCEe1t9X-2m__44zIFfBwkpqaa2xFrpB7CnYzI130_provenance.
- befree-2016 importedOn "2016-02-19" NP661717.RA0zvAxOCEe1t9X-2m__44zIFfBwkpqaa2xFrpB7CnYzI130_provenance.