Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP493821.RAnt1CGJTZGpZBj0QJfbvnnu8ekh0rRNdiPQ-K_G1i1ho130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP493821.RAnt1CGJTZGpZBj0QJfbvnnu8ekh0rRNdiPQ-K_G1i1ho130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP493821.RAnt1CGJTZGpZBj0QJfbvnnu8ekh0rRNdiPQ-K_G1i1ho130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP493821.RAnt1CGJTZGpZBj0QJfbvnnu8ekh0rRNdiPQ-K_G1i1ho130_provenance.
- NP493821.RAnt1CGJTZGpZBj0QJfbvnnu8ekh0rRNdiPQ-K_G1i1ho130_assertion description "[Women with a heterozygous genotype had no greater risk whereas those with a homozygous variant genotype had a greater risk than women with a wild-type genotype for the MDM2 SNP309 (covariate-adjusted odds ratio, 1.87; 95% confidence interval, 1.29-2.73) for endometrial cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP493821.RAnt1CGJTZGpZBj0QJfbvnnu8ekh0rRNdiPQ-K_G1i1ho130_provenance.
- NP493821.RAnt1CGJTZGpZBj0QJfbvnnu8ekh0rRNdiPQ-K_G1i1ho130_assertion evidence source_evidence_literature NP493821.RAnt1CGJTZGpZBj0QJfbvnnu8ekh0rRNdiPQ-K_G1i1ho130_provenance.
- NP493821.RAnt1CGJTZGpZBj0QJfbvnnu8ekh0rRNdiPQ-K_G1i1ho130_assertion SIO_000772 18398041 NP493821.RAnt1CGJTZGpZBj0QJfbvnnu8ekh0rRNdiPQ-K_G1i1ho130_provenance.
- NP493821.RAnt1CGJTZGpZBj0QJfbvnnu8ekh0rRNdiPQ-K_G1i1ho130_assertion wasDerivedFrom befree-20140225 NP493821.RAnt1CGJTZGpZBj0QJfbvnnu8ekh0rRNdiPQ-K_G1i1ho130_provenance.
- NP493821.RAnt1CGJTZGpZBj0QJfbvnnu8ekh0rRNdiPQ-K_G1i1ho130_assertion wasGeneratedBy ECO_0000203 NP493821.RAnt1CGJTZGpZBj0QJfbvnnu8ekh0rRNdiPQ-K_G1i1ho130_provenance.
- befree-20140225 importedOn "2014-02-25" NP493821.RAnt1CGJTZGpZBj0QJfbvnnu8ekh0rRNdiPQ-K_G1i1ho130_provenance.