Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP570141.RArFKnqO7CAtrT8ICU-r7tvOStxwykSk58XuDt-Im-OZ4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP570141.RArFKnqO7CAtrT8ICU-r7tvOStxwykSk58XuDt-Im-OZ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP570141.RArFKnqO7CAtrT8ICU-r7tvOStxwykSk58XuDt-Im-OZ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP570141.RArFKnqO7CAtrT8ICU-r7tvOStxwykSk58XuDt-Im-OZ4130_provenance.
- NP570141.RArFKnqO7CAtrT8ICU-r7tvOStxwykSk58XuDt-Im-OZ4130_assertion description "[Among white women, the frequency of the 3'UTR/T allele carriers (TC+TT genotypes) increased gradually from 67.9% to 75.0% and 79.2% in the <20%, 20% to 49%, and >or=50% stenosis groups, respectively (chi2 trend=6.23; P=0.013).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP570141.RArFKnqO7CAtrT8ICU-r7tvOStxwykSk58XuDt-Im-OZ4130_provenance.
- NP570141.RArFKnqO7CAtrT8ICU-r7tvOStxwykSk58XuDt-Im-OZ4130_assertion evidence source_evidence_literature NP570141.RArFKnqO7CAtrT8ICU-r7tvOStxwykSk58XuDt-Im-OZ4130_provenance.
- NP570141.RArFKnqO7CAtrT8ICU-r7tvOStxwykSk58XuDt-Im-OZ4130_assertion SIO_000772 12810610 NP570141.RArFKnqO7CAtrT8ICU-r7tvOStxwykSk58XuDt-Im-OZ4130_provenance.
- NP570141.RArFKnqO7CAtrT8ICU-r7tvOStxwykSk58XuDt-Im-OZ4130_assertion wasDerivedFrom befree-20140225 NP570141.RArFKnqO7CAtrT8ICU-r7tvOStxwykSk58XuDt-Im-OZ4130_provenance.
- NP570141.RArFKnqO7CAtrT8ICU-r7tvOStxwykSk58XuDt-Im-OZ4130_assertion wasGeneratedBy ECO_0000203 NP570141.RArFKnqO7CAtrT8ICU-r7tvOStxwykSk58XuDt-Im-OZ4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP570141.RArFKnqO7CAtrT8ICU-r7tvOStxwykSk58XuDt-Im-OZ4130_provenance.