Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP887949.RAxaLZx7KsHxCuRbj6TYNaYu7RxQsbNSYJGVlLxrE9o5A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP887949.RAxaLZx7KsHxCuRbj6TYNaYu7RxQsbNSYJGVlLxrE9o5A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP887949.RAxaLZx7KsHxCuRbj6TYNaYu7RxQsbNSYJGVlLxrE9o5A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP887949.RAxaLZx7KsHxCuRbj6TYNaYu7RxQsbNSYJGVlLxrE9o5A130_provenance.
- NP887949.RAxaLZx7KsHxCuRbj6TYNaYu7RxQsbNSYJGVlLxrE9o5A130_assertion description "[The aim of the present study was to test for an association between the CFH-Y402H variant and MI in a large case-control sample with a familial background for CAD (coronary artery disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887949.RAxaLZx7KsHxCuRbj6TYNaYu7RxQsbNSYJGVlLxrE9o5A130_provenance.
- NP887949.RAxaLZx7KsHxCuRbj6TYNaYu7RxQsbNSYJGVlLxrE9o5A130_assertion evidence source_evidence_literature NP887949.RAxaLZx7KsHxCuRbj6TYNaYu7RxQsbNSYJGVlLxrE9o5A130_provenance.
- NP887949.RAxaLZx7KsHxCuRbj6TYNaYu7RxQsbNSYJGVlLxrE9o5A130_assertion SIO_000772 17472578 NP887949.RAxaLZx7KsHxCuRbj6TYNaYu7RxQsbNSYJGVlLxrE9o5A130_provenance.
- NP887949.RAxaLZx7KsHxCuRbj6TYNaYu7RxQsbNSYJGVlLxrE9o5A130_assertion wasDerivedFrom befree-20140225 NP887949.RAxaLZx7KsHxCuRbj6TYNaYu7RxQsbNSYJGVlLxrE9o5A130_provenance.
- NP887949.RAxaLZx7KsHxCuRbj6TYNaYu7RxQsbNSYJGVlLxrE9o5A130_assertion wasGeneratedBy ECO_0000203 NP887949.RAxaLZx7KsHxCuRbj6TYNaYu7RxQsbNSYJGVlLxrE9o5A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP887949.RAxaLZx7KsHxCuRbj6TYNaYu7RxQsbNSYJGVlLxrE9o5A130_provenance.