Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP968621.RAwkJe6VNdFZ3UV9ycqJG-3lCeuQLH8Eby2sRfEXlTWXI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP968621.RAwkJe6VNdFZ3UV9ycqJG-3lCeuQLH8Eby2sRfEXlTWXI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP968621.RAwkJe6VNdFZ3UV9ycqJG-3lCeuQLH8Eby2sRfEXlTWXI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP968621.RAwkJe6VNdFZ3UV9ycqJG-3lCeuQLH8Eby2sRfEXlTWXI130_provenance.
- NP968621.RAwkJe6VNdFZ3UV9ycqJG-3lCeuQLH8Eby2sRfEXlTWXI130_assertion description "[A haplotype of -1195G, -765G and 8160A alleles was associated with a modest increase in the risk (adjusted odds ratio [OR] 1.38, 95% confidence interval [CI] 0.99-1.91), and the increase was more evident for distal adenomas (adjusted OR 1.57, 95% CI 1.04-2.38).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP968621.RAwkJe6VNdFZ3UV9ycqJG-3lCeuQLH8Eby2sRfEXlTWXI130_provenance.
- NP968621.RAwkJe6VNdFZ3UV9ycqJG-3lCeuQLH8Eby2sRfEXlTWXI130_assertion evidence source_evidence_literature NP968621.RAwkJe6VNdFZ3UV9ycqJG-3lCeuQLH8Eby2sRfEXlTWXI130_provenance.
- NP968621.RAwkJe6VNdFZ3UV9ycqJG-3lCeuQLH8Eby2sRfEXlTWXI130_assertion SIO_000772 18167131 NP968621.RAwkJe6VNdFZ3UV9ycqJG-3lCeuQLH8Eby2sRfEXlTWXI130_provenance.
- NP968621.RAwkJe6VNdFZ3UV9ycqJG-3lCeuQLH8Eby2sRfEXlTWXI130_assertion wasDerivedFrom befree-20150227 NP968621.RAwkJe6VNdFZ3UV9ycqJG-3lCeuQLH8Eby2sRfEXlTWXI130_provenance.
- NP968621.RAwkJe6VNdFZ3UV9ycqJG-3lCeuQLH8Eby2sRfEXlTWXI130_assertion wasGeneratedBy ECO_0000203 NP968621.RAwkJe6VNdFZ3UV9ycqJG-3lCeuQLH8Eby2sRfEXlTWXI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP968621.RAwkJe6VNdFZ3UV9ycqJG-3lCeuQLH8Eby2sRfEXlTWXI130_provenance.