Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP497565.RAvImLe4IrxuHSlvBQSu-aDvz405bfFzd3ihLtJdnJeOk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP497565.RAvImLe4IrxuHSlvBQSu-aDvz405bfFzd3ihLtJdnJeOk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP497565.RAvImLe4IrxuHSlvBQSu-aDvz405bfFzd3ihLtJdnJeOk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP497565.RAvImLe4IrxuHSlvBQSu-aDvz405bfFzd3ihLtJdnJeOk130_provenance.
- NP497565.RAvImLe4IrxuHSlvBQSu-aDvz405bfFzd3ihLtJdnJeOk130_assertion description "[The XRCC1 codon 399 Gln/Gln genotype was significantly associated with reduced risk of ESQCC (OR = 0.31, 95% CI = 0.12-0.78, P = 0.01).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP497565.RAvImLe4IrxuHSlvBQSu-aDvz405bfFzd3ihLtJdnJeOk130_provenance.
- NP497565.RAvImLe4IrxuHSlvBQSu-aDvz405bfFzd3ihLtJdnJeOk130_assertion evidence source_evidence_literature NP497565.RAvImLe4IrxuHSlvBQSu-aDvz405bfFzd3ihLtJdnJeOk130_provenance.
- NP497565.RAvImLe4IrxuHSlvBQSu-aDvz405bfFzd3ihLtJdnJeOk130_assertion SIO_000772 17556064 NP497565.RAvImLe4IrxuHSlvBQSu-aDvz405bfFzd3ihLtJdnJeOk130_provenance.
- NP497565.RAvImLe4IrxuHSlvBQSu-aDvz405bfFzd3ihLtJdnJeOk130_assertion wasDerivedFrom befree-20140225 NP497565.RAvImLe4IrxuHSlvBQSu-aDvz405bfFzd3ihLtJdnJeOk130_provenance.
- NP497565.RAvImLe4IrxuHSlvBQSu-aDvz405bfFzd3ihLtJdnJeOk130_assertion wasGeneratedBy ECO_0000203 NP497565.RAvImLe4IrxuHSlvBQSu-aDvz405bfFzd3ihLtJdnJeOk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP497565.RAvImLe4IrxuHSlvBQSu-aDvz405bfFzd3ihLtJdnJeOk130_provenance.