Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1130128.RAz73q5P4hOGpQzHThqLqsvKGBmteiyVLZ309jAWJXf9k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1130128.RAz73q5P4hOGpQzHThqLqsvKGBmteiyVLZ309jAWJXf9k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1130128.RAz73q5P4hOGpQzHThqLqsvKGBmteiyVLZ309jAWJXf9k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1130128.RAz73q5P4hOGpQzHThqLqsvKGBmteiyVLZ309jAWJXf9k130_provenance.
- NP1130128.RAz73q5P4hOGpQzHThqLqsvKGBmteiyVLZ309jAWJXf9k130_assertion description "[Two non-synonymous SNPs, rs12075 (G42D) in DARC and rs2228468 (S373Y) in CCBP2, were observed to be associated with LNM in univariate analysis and remained significant after adjustment for conventional clinical risk factors, with odds ratios (ORs) of 0.54 (95% confidence interval [CI], 0.37 to 0.79) and 0.78 (95% CI, 0.62 to 0.98), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1130128.RAz73q5P4hOGpQzHThqLqsvKGBmteiyVLZ309jAWJXf9k130_provenance.
- NP1130128.RAz73q5P4hOGpQzHThqLqsvKGBmteiyVLZ309jAWJXf9k130_assertion evidence source_evidence_literature NP1130128.RAz73q5P4hOGpQzHThqLqsvKGBmteiyVLZ309jAWJXf9k130_provenance.
- NP1130128.RAz73q5P4hOGpQzHThqLqsvKGBmteiyVLZ309jAWJXf9k130_assertion SIO_000772 24260134 NP1130128.RAz73q5P4hOGpQzHThqLqsvKGBmteiyVLZ309jAWJXf9k130_provenance.
- NP1130128.RAz73q5P4hOGpQzHThqLqsvKGBmteiyVLZ309jAWJXf9k130_assertion wasDerivedFrom befree-2016 NP1130128.RAz73q5P4hOGpQzHThqLqsvKGBmteiyVLZ309jAWJXf9k130_provenance.
- NP1130128.RAz73q5P4hOGpQzHThqLqsvKGBmteiyVLZ309jAWJXf9k130_assertion wasGeneratedBy ECO_0000203 NP1130128.RAz73q5P4hOGpQzHThqLqsvKGBmteiyVLZ309jAWJXf9k130_provenance.
- befree-2016 importedOn "2016-02-19" NP1130128.RAz73q5P4hOGpQzHThqLqsvKGBmteiyVLZ309jAWJXf9k130_provenance.