Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP527080.RASORzmXSMUJn_ANEvzecD_28X5y3Nn-tql79X1md-F9Y130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP527080.RASORzmXSMUJn_ANEvzecD_28X5y3Nn-tql79X1md-F9Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP527080.RASORzmXSMUJn_ANEvzecD_28X5y3Nn-tql79X1md-F9Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP527080.RASORzmXSMUJn_ANEvzecD_28X5y3Nn-tql79X1md-F9Y130_provenance.
- NP527080.RASORzmXSMUJn_ANEvzecD_28X5y3Nn-tql79X1md-F9Y130_assertion description "[This study was undertaken to determine the spectrum and prevalence of mutations in the RYR2-encoded cardiac ryanodine receptor in cases with exertional syncope and normal corrected QT interval (QTc).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP527080.RASORzmXSMUJn_ANEvzecD_28X5y3Nn-tql79X1md-F9Y130_provenance.
- NP527080.RASORzmXSMUJn_ANEvzecD_28X5y3Nn-tql79X1md-F9Y130_assertion evidence source_evidence_literature NP527080.RASORzmXSMUJn_ANEvzecD_28X5y3Nn-tql79X1md-F9Y130_provenance.
- NP527080.RASORzmXSMUJn_ANEvzecD_28X5y3Nn-tql79X1md-F9Y130_assertion SIO_000772 19926015 NP527080.RASORzmXSMUJn_ANEvzecD_28X5y3Nn-tql79X1md-F9Y130_provenance.
- NP527080.RASORzmXSMUJn_ANEvzecD_28X5y3Nn-tql79X1md-F9Y130_assertion wasDerivedFrom befree-20140225 NP527080.RASORzmXSMUJn_ANEvzecD_28X5y3Nn-tql79X1md-F9Y130_provenance.
- NP527080.RASORzmXSMUJn_ANEvzecD_28X5y3Nn-tql79X1md-F9Y130_assertion wasGeneratedBy ECO_0000203 NP527080.RASORzmXSMUJn_ANEvzecD_28X5y3Nn-tql79X1md-F9Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP527080.RASORzmXSMUJn_ANEvzecD_28X5y3Nn-tql79X1md-F9Y130_provenance.