Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP697561.RAv5TH0OXi701e1EcrXiTF4HHdAZDK-0iO_XtR5mO96_k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP697561.RAv5TH0OXi701e1EcrXiTF4HHdAZDK-0iO_XtR5mO96_k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP697561.RAv5TH0OXi701e1EcrXiTF4HHdAZDK-0iO_XtR5mO96_k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP697561.RAv5TH0OXi701e1EcrXiTF4HHdAZDK-0iO_XtR5mO96_k130_provenance.
- NP697561.RAv5TH0OXi701e1EcrXiTF4HHdAZDK-0iO_XtR5mO96_k130_assertion description "[Mutations in PRKAG2, the gene for the gamma 2 regulatory subunit of AMP-activated protein kinase, cause cardiac hypertrophy and electrophysiologic abnormalities, particularly preexcitation (Wolff-Parkinson-White syndrome) and atrioventricular conduction block.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP697561.RAv5TH0OXi701e1EcrXiTF4HHdAZDK-0iO_XtR5mO96_k130_provenance.
- NP697561.RAv5TH0OXi701e1EcrXiTF4HHdAZDK-0iO_XtR5mO96_k130_assertion evidence source_evidence_literature NP697561.RAv5TH0OXi701e1EcrXiTF4HHdAZDK-0iO_XtR5mO96_k130_provenance.
- NP697561.RAv5TH0OXi701e1EcrXiTF4HHdAZDK-0iO_XtR5mO96_k130_assertion SIO_000772 11827995 NP697561.RAv5TH0OXi701e1EcrXiTF4HHdAZDK-0iO_XtR5mO96_k130_provenance.
- NP697561.RAv5TH0OXi701e1EcrXiTF4HHdAZDK-0iO_XtR5mO96_k130_assertion wasDerivedFrom befree-20140225 NP697561.RAv5TH0OXi701e1EcrXiTF4HHdAZDK-0iO_XtR5mO96_k130_provenance.
- NP697561.RAv5TH0OXi701e1EcrXiTF4HHdAZDK-0iO_XtR5mO96_k130_assertion wasGeneratedBy ECO_0000203 NP697561.RAv5TH0OXi701e1EcrXiTF4HHdAZDK-0iO_XtR5mO96_k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP697561.RAv5TH0OXi701e1EcrXiTF4HHdAZDK-0iO_XtR5mO96_k130_provenance.