Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP616648.RADs0991XhNuizgyd2ibXxHNxOt-Dv1BTsoWmqgKXiDiQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP616648.RADs0991XhNuizgyd2ibXxHNxOt-Dv1BTsoWmqgKXiDiQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP616648.RADs0991XhNuizgyd2ibXxHNxOt-Dv1BTsoWmqgKXiDiQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP616648.RADs0991XhNuizgyd2ibXxHNxOt-Dv1BTsoWmqgKXiDiQ130_provenance.
- NP616648.RADs0991XhNuizgyd2ibXxHNxOt-Dv1BTsoWmqgKXiDiQ130_assertion description "[A decrease in CAD patients carrying the CAC haplotype compared to controls (p=0.043) and a decrease in the CAC haplotype in CAD patients with hypertension vs healthy controls (p=0.029) were demonstrated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616648.RADs0991XhNuizgyd2ibXxHNxOt-Dv1BTsoWmqgKXiDiQ130_provenance.
- NP616648.RADs0991XhNuizgyd2ibXxHNxOt-Dv1BTsoWmqgKXiDiQ130_assertion evidence source_evidence_literature NP616648.RADs0991XhNuizgyd2ibXxHNxOt-Dv1BTsoWmqgKXiDiQ130_provenance.
- NP616648.RADs0991XhNuizgyd2ibXxHNxOt-Dv1BTsoWmqgKXiDiQ130_assertion SIO_000772 19578791 NP616648.RADs0991XhNuizgyd2ibXxHNxOt-Dv1BTsoWmqgKXiDiQ130_provenance.
- NP616648.RADs0991XhNuizgyd2ibXxHNxOt-Dv1BTsoWmqgKXiDiQ130_assertion wasDerivedFrom befree-20140225 NP616648.RADs0991XhNuizgyd2ibXxHNxOt-Dv1BTsoWmqgKXiDiQ130_provenance.
- NP616648.RADs0991XhNuizgyd2ibXxHNxOt-Dv1BTsoWmqgKXiDiQ130_assertion wasGeneratedBy ECO_0000203 NP616648.RADs0991XhNuizgyd2ibXxHNxOt-Dv1BTsoWmqgKXiDiQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP616648.RADs0991XhNuizgyd2ibXxHNxOt-Dv1BTsoWmqgKXiDiQ130_provenance.