Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP351292.RAa1GU-pMzC6Hx2LJwrLld65R_gh-EPApiWe08po7mQLA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP351292.RAa1GU-pMzC6Hx2LJwrLld65R_gh-EPApiWe08po7mQLA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP351292.RAa1GU-pMzC6Hx2LJwrLld65R_gh-EPApiWe08po7mQLA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP351292.RAa1GU-pMzC6Hx2LJwrLld65R_gh-EPApiWe08po7mQLA130_provenance.
- NP351292.RAa1GU-pMzC6Hx2LJwrLld65R_gh-EPApiWe08po7mQLA130_assertion description "[The minor allele frequency for rs7903146 was different between TCP and FCPD patients carrying the N34S SPINK1 variant but did not reach statistical significance (OR = 1.59, 95% CI = 0.93-2.70, P = 0.09), while, TCF7L2variant showed a statistically significant association between TCP and FCPD patients carrying the 26V allele (OR = 1.69, 95% CI = 1.11-2.56, P = 0.013).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351292.RAa1GU-pMzC6Hx2LJwrLld65R_gh-EPApiWe08po7mQLA130_provenance.
- NP351292.RAa1GU-pMzC6Hx2LJwrLld65R_gh-EPApiWe08po7mQLA130_assertion evidence source_evidence_literature NP351292.RAa1GU-pMzC6Hx2LJwrLld65R_gh-EPApiWe08po7mQLA130_provenance.
- NP351292.RAa1GU-pMzC6Hx2LJwrLld65R_gh-EPApiWe08po7mQLA130_assertion SIO_000772 18706099 NP351292.RAa1GU-pMzC6Hx2LJwrLld65R_gh-EPApiWe08po7mQLA130_provenance.
- NP351292.RAa1GU-pMzC6Hx2LJwrLld65R_gh-EPApiWe08po7mQLA130_assertion wasDerivedFrom befree-20140225 NP351292.RAa1GU-pMzC6Hx2LJwrLld65R_gh-EPApiWe08po7mQLA130_provenance.
- NP351292.RAa1GU-pMzC6Hx2LJwrLld65R_gh-EPApiWe08po7mQLA130_assertion wasGeneratedBy ECO_0000203 NP351292.RAa1GU-pMzC6Hx2LJwrLld65R_gh-EPApiWe08po7mQLA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP351292.RAa1GU-pMzC6Hx2LJwrLld65R_gh-EPApiWe08po7mQLA130_provenance.