Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP900092.RAhs_ujX7NW2Wnbxy0kOsqlajWCp0AtyfLtPV17UPaxgI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP900092.RAhs_ujX7NW2Wnbxy0kOsqlajWCp0AtyfLtPV17UPaxgI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP900092.RAhs_ujX7NW2Wnbxy0kOsqlajWCp0AtyfLtPV17UPaxgI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP900092.RAhs_ujX7NW2Wnbxy0kOsqlajWCp0AtyfLtPV17UPaxgI130_provenance.
- NP900092.RAhs_ujX7NW2Wnbxy0kOsqlajWCp0AtyfLtPV17UPaxgI130_assertion description "[We studied the prevalence, clinical phenotypes, and risk of SCD presented by ten rare mutations previously associated with arrhythmogenic right ventricular cardiomyopathy, long QT syndrome, or catecholaminergic polymorphic ventricular tachycardia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP900092.RAhs_ujX7NW2Wnbxy0kOsqlajWCp0AtyfLtPV17UPaxgI130_provenance.
- NP900092.RAhs_ujX7NW2Wnbxy0kOsqlajWCp0AtyfLtPV17UPaxgI130_assertion evidence source_evidence_literature NP900092.RAhs_ujX7NW2Wnbxy0kOsqlajWCp0AtyfLtPV17UPaxgI130_provenance.
- NP900092.RAhs_ujX7NW2Wnbxy0kOsqlajWCp0AtyfLtPV17UPaxgI130_assertion SIO_000772 23651034 NP900092.RAhs_ujX7NW2Wnbxy0kOsqlajWCp0AtyfLtPV17UPaxgI130_provenance.
- NP900092.RAhs_ujX7NW2Wnbxy0kOsqlajWCp0AtyfLtPV17UPaxgI130_assertion wasDerivedFrom befree-20140225 NP900092.RAhs_ujX7NW2Wnbxy0kOsqlajWCp0AtyfLtPV17UPaxgI130_provenance.
- NP900092.RAhs_ujX7NW2Wnbxy0kOsqlajWCp0AtyfLtPV17UPaxgI130_assertion wasGeneratedBy ECO_0000203 NP900092.RAhs_ujX7NW2Wnbxy0kOsqlajWCp0AtyfLtPV17UPaxgI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP900092.RAhs_ujX7NW2Wnbxy0kOsqlajWCp0AtyfLtPV17UPaxgI130_provenance.