Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP342999.RA1S4MpPNgRN-U41iSKkKmUJG7ND1HzMahGKw_TVFcqYc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP342999.RA1S4MpPNgRN-U41iSKkKmUJG7ND1HzMahGKw_TVFcqYc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP342999.RA1S4MpPNgRN-U41iSKkKmUJG7ND1HzMahGKw_TVFcqYc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP342999.RA1S4MpPNgRN-U41iSKkKmUJG7ND1HzMahGKw_TVFcqYc130_provenance.
- NP342999.RA1S4MpPNgRN-U41iSKkKmUJG7ND1HzMahGKw_TVFcqYc130_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." NP342999.RA1S4MpPNgRN-U41iSKkKmUJG7ND1HzMahGKw_TVFcqYc130_provenance.
- NP342999.RA1S4MpPNgRN-U41iSKkKmUJG7ND1HzMahGKw_TVFcqYc130_assertion evidence source_evidence_literature NP342999.RA1S4MpPNgRN-U41iSKkKmUJG7ND1HzMahGKw_TVFcqYc130_provenance.
- NP342999.RA1S4MpPNgRN-U41iSKkKmUJG7ND1HzMahGKw_TVFcqYc130_assertion SIO_000772 11807805 NP342999.RA1S4MpPNgRN-U41iSKkKmUJG7ND1HzMahGKw_TVFcqYc130_provenance.
- NP342999.RA1S4MpPNgRN-U41iSKkKmUJG7ND1HzMahGKw_TVFcqYc130_assertion wasDerivedFrom befree-2016 NP342999.RA1S4MpPNgRN-U41iSKkKmUJG7ND1HzMahGKw_TVFcqYc130_provenance.
- NP342999.RA1S4MpPNgRN-U41iSKkKmUJG7ND1HzMahGKw_TVFcqYc130_assertion wasGeneratedBy ECO_0000203 NP342999.RA1S4MpPNgRN-U41iSKkKmUJG7ND1HzMahGKw_TVFcqYc130_provenance.
- befree-2016 importedOn "2016-02-19" NP342999.RA1S4MpPNgRN-U41iSKkKmUJG7ND1HzMahGKw_TVFcqYc130_provenance.