Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP946650.RAdk3xabBs-bdM6wjqMWmdMWotnN21tQKhBPgwFXHL6PY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP946650.RAdk3xabBs-bdM6wjqMWmdMWotnN21tQKhBPgwFXHL6PY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP946650.RAdk3xabBs-bdM6wjqMWmdMWotnN21tQKhBPgwFXHL6PY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP946650.RAdk3xabBs-bdM6wjqMWmdMWotnN21tQKhBPgwFXHL6PY130_provenance.
- NP946650.RAdk3xabBs-bdM6wjqMWmdMWotnN21tQKhBPgwFXHL6PY130_assertion description "[A SNP-based analysis showed that a C>T base substitution for C1RL rs3813729 (odds ratio (OR)(CT) = 0.60, 95% confidence interval (CI) = 0.42-0.87, P(trend) = 0.0062) was associated with a decreased risk of overall NHL, as well as for DLBCL (OR(CT) = 0.39, 95% CI = 0.20-0.73; P(trend) = 0.0034).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP946650.RAdk3xabBs-bdM6wjqMWmdMWotnN21tQKhBPgwFXHL6PY130_provenance.
- NP946650.RAdk3xabBs-bdM6wjqMWmdMWotnN21tQKhBPgwFXHL6PY130_assertion evidence source_evidence_literature NP946650.RAdk3xabBs-bdM6wjqMWmdMWotnN21tQKhBPgwFXHL6PY130_provenance.
- NP946650.RAdk3xabBs-bdM6wjqMWmdMWotnN21tQKhBPgwFXHL6PY130_assertion SIO_000772 22170086 NP946650.RAdk3xabBs-bdM6wjqMWmdMWotnN21tQKhBPgwFXHL6PY130_provenance.
- NP946650.RAdk3xabBs-bdM6wjqMWmdMWotnN21tQKhBPgwFXHL6PY130_assertion wasDerivedFrom befree-2016 NP946650.RAdk3xabBs-bdM6wjqMWmdMWotnN21tQKhBPgwFXHL6PY130_provenance.
- NP946650.RAdk3xabBs-bdM6wjqMWmdMWotnN21tQKhBPgwFXHL6PY130_assertion wasGeneratedBy ECO_0000203 NP946650.RAdk3xabBs-bdM6wjqMWmdMWotnN21tQKhBPgwFXHL6PY130_provenance.
- befree-2016 importedOn "2016-02-19" NP946650.RAdk3xabBs-bdM6wjqMWmdMWotnN21tQKhBPgwFXHL6PY130_provenance.