Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP903758.RAON8MOm0Ml54sf9TWk6OXhq83-cjwifK0PaFmTBxsnvU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP903758.RAON8MOm0Ml54sf9TWk6OXhq83-cjwifK0PaFmTBxsnvU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP903758.RAON8MOm0Ml54sf9TWk6OXhq83-cjwifK0PaFmTBxsnvU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP903758.RAON8MOm0Ml54sf9TWk6OXhq83-cjwifK0PaFmTBxsnvU130_provenance.
- NP903758.RAON8MOm0Ml54sf9TWk6OXhq83-cjwifK0PaFmTBxsnvU130_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." NP903758.RAON8MOm0Ml54sf9TWk6OXhq83-cjwifK0PaFmTBxsnvU130_provenance.
- NP903758.RAON8MOm0Ml54sf9TWk6OXhq83-cjwifK0PaFmTBxsnvU130_assertion evidence source_evidence_literature NP903758.RAON8MOm0Ml54sf9TWk6OXhq83-cjwifK0PaFmTBxsnvU130_provenance.
- NP903758.RAON8MOm0Ml54sf9TWk6OXhq83-cjwifK0PaFmTBxsnvU130_assertion SIO_000772 22170086 NP903758.RAON8MOm0Ml54sf9TWk6OXhq83-cjwifK0PaFmTBxsnvU130_provenance.
- NP903758.RAON8MOm0Ml54sf9TWk6OXhq83-cjwifK0PaFmTBxsnvU130_assertion wasDerivedFrom befree-20150227 NP903758.RAON8MOm0Ml54sf9TWk6OXhq83-cjwifK0PaFmTBxsnvU130_provenance.
- NP903758.RAON8MOm0Ml54sf9TWk6OXhq83-cjwifK0PaFmTBxsnvU130_assertion wasGeneratedBy ECO_0000203 NP903758.RAON8MOm0Ml54sf9TWk6OXhq83-cjwifK0PaFmTBxsnvU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP903758.RAON8MOm0Ml54sf9TWk6OXhq83-cjwifK0PaFmTBxsnvU130_provenance.