Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP677101.RAAFjcFzTg2HpQbRhCNlIdSPlScL4nNQQpZf21kM76cqQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP677101.RAAFjcFzTg2HpQbRhCNlIdSPlScL4nNQQpZf21kM76cqQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP677101.RAAFjcFzTg2HpQbRhCNlIdSPlScL4nNQQpZf21kM76cqQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP677101.RAAFjcFzTg2HpQbRhCNlIdSPlScL4nNQQpZf21kM76cqQ130_provenance.
- NP677101.RAAFjcFzTg2HpQbRhCNlIdSPlScL4nNQQpZf21kM76cqQ130_assertion description "[The cardiac ryanodine receptor (RyR2), the major calcium release channel on the sarcoplasmic reticulum (SR) in cardiomyocytes, has recently been shown to be involved in at least two forms of sudden cardiac death (SCD): (1) Catecholaminergic polymorphic ventricular tachycardia (CPVT) or familial polymorphic VT (FPVT); and (2) Arrhythmogenic right ventricular dysplasia type 2 (ARVD2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP677101.RAAFjcFzTg2HpQbRhCNlIdSPlScL4nNQQpZf21kM76cqQ130_provenance.
- NP677101.RAAFjcFzTg2HpQbRhCNlIdSPlScL4nNQQpZf21kM76cqQ130_assertion evidence source_evidence_literature NP677101.RAAFjcFzTg2HpQbRhCNlIdSPlScL4nNQQpZf21kM76cqQ130_provenance.
- NP677101.RAAFjcFzTg2HpQbRhCNlIdSPlScL4nNQQpZf21kM76cqQ130_assertion SIO_000772 11807805 NP677101.RAAFjcFzTg2HpQbRhCNlIdSPlScL4nNQQpZf21kM76cqQ130_provenance.
- NP677101.RAAFjcFzTg2HpQbRhCNlIdSPlScL4nNQQpZf21kM76cqQ130_assertion wasDerivedFrom befree-20150227 NP677101.RAAFjcFzTg2HpQbRhCNlIdSPlScL4nNQQpZf21kM76cqQ130_provenance.
- NP677101.RAAFjcFzTg2HpQbRhCNlIdSPlScL4nNQQpZf21kM76cqQ130_assertion wasGeneratedBy ECO_0000203 NP677101.RAAFjcFzTg2HpQbRhCNlIdSPlScL4nNQQpZf21kM76cqQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP677101.RAAFjcFzTg2HpQbRhCNlIdSPlScL4nNQQpZf21kM76cqQ130_provenance.