Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP208278.RACbRPMRSBSOYelzf6VofIierGSpJFS0tpzhQABfoWDBk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP208278.RACbRPMRSBSOYelzf6VofIierGSpJFS0tpzhQABfoWDBk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP208278.RACbRPMRSBSOYelzf6VofIierGSpJFS0tpzhQABfoWDBk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP208278.RACbRPMRSBSOYelzf6VofIierGSpJFS0tpzhQABfoWDBk130_provenance.
- NP208278.RACbRPMRSBSOYelzf6VofIierGSpJFS0tpzhQABfoWDBk130_assertion description "[After adjusting for sex, age at RA diagnosis and traditional CV risk factors RA patients carrying the NFKB1 del/del genotype had higher risk of CV events than those with ins/ins genotype (Hazard ratio [HR] = 1.76, 95% CI: 1.05-2.97, p = 0.03), while heterozygous patients had an intermediate (but non-significant) risk (HR = 1.31, 95% CI: 0.90-1.92, p = 0.16).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208278.RACbRPMRSBSOYelzf6VofIierGSpJFS0tpzhQABfoWDBk130_provenance.
- NP208278.RACbRPMRSBSOYelzf6VofIierGSpJFS0tpzhQABfoWDBk130_assertion evidence source_evidence_literature NP208278.RACbRPMRSBSOYelzf6VofIierGSpJFS0tpzhQABfoWDBk130_provenance.
- NP208278.RACbRPMRSBSOYelzf6VofIierGSpJFS0tpzhQABfoWDBk130_assertion SIO_000772 22742859 NP208278.RACbRPMRSBSOYelzf6VofIierGSpJFS0tpzhQABfoWDBk130_provenance.
- NP208278.RACbRPMRSBSOYelzf6VofIierGSpJFS0tpzhQABfoWDBk130_assertion wasDerivedFrom befree-20140225 NP208278.RACbRPMRSBSOYelzf6VofIierGSpJFS0tpzhQABfoWDBk130_provenance.
- NP208278.RACbRPMRSBSOYelzf6VofIierGSpJFS0tpzhQABfoWDBk130_assertion wasGeneratedBy ECO_0000203 NP208278.RACbRPMRSBSOYelzf6VofIierGSpJFS0tpzhQABfoWDBk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP208278.RACbRPMRSBSOYelzf6VofIierGSpJFS0tpzhQABfoWDBk130_provenance.