Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP968693.RACn_eeuaaNmGXqV_G3ci7uPMNllfUKh11cyHDBLFFN0M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP968693.RACn_eeuaaNmGXqV_G3ci7uPMNllfUKh11cyHDBLFFN0M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP968693.RACn_eeuaaNmGXqV_G3ci7uPMNllfUKh11cyHDBLFFN0M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP968693.RACn_eeuaaNmGXqV_G3ci7uPMNllfUKh11cyHDBLFFN0M130_provenance.
- NP968693.RACn_eeuaaNmGXqV_G3ci7uPMNllfUKh11cyHDBLFFN0M130_assertion description "[The deletion of LCE3C_LCE3B and SNPs rs4112788 and rs4085613 showed an association with RA (allele analysis: p=7.72�10(-4), OR 1.28, 95% CI 1.11 to 1.47; p=6.39�10(-4), OR 1.23, 95% CI 1.09 to 1.38; and p=5.38�10(-4), OR 1.23, 95% CI 1.10 to 1.39, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP968693.RACn_eeuaaNmGXqV_G3ci7uPMNllfUKh11cyHDBLFFN0M130_provenance.
- NP968693.RACn_eeuaaNmGXqV_G3ci7uPMNllfUKh11cyHDBLFFN0M130_assertion evidence source_evidence_literature NP968693.RACn_eeuaaNmGXqV_G3ci7uPMNllfUKh11cyHDBLFFN0M130_provenance.
- NP968693.RACn_eeuaaNmGXqV_G3ci7uPMNllfUKh11cyHDBLFFN0M130_assertion SIO_000772 21628307 NP968693.RACn_eeuaaNmGXqV_G3ci7uPMNllfUKh11cyHDBLFFN0M130_provenance.
- NP968693.RACn_eeuaaNmGXqV_G3ci7uPMNllfUKh11cyHDBLFFN0M130_assertion wasDerivedFrom befree-20150227 NP968693.RACn_eeuaaNmGXqV_G3ci7uPMNllfUKh11cyHDBLFFN0M130_provenance.
- NP968693.RACn_eeuaaNmGXqV_G3ci7uPMNllfUKh11cyHDBLFFN0M130_assertion wasGeneratedBy ECO_0000203 NP968693.RACn_eeuaaNmGXqV_G3ci7uPMNllfUKh11cyHDBLFFN0M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP968693.RACn_eeuaaNmGXqV_G3ci7uPMNllfUKh11cyHDBLFFN0M130_provenance.