Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP676829.RADgcGo2YXl_66B1nU6zvxgyot8y_CR2wcNTGeDvRLCow130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP676829.RADgcGo2YXl_66B1nU6zvxgyot8y_CR2wcNTGeDvRLCow130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP676829.RADgcGo2YXl_66B1nU6zvxgyot8y_CR2wcNTGeDvRLCow130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP676829.RADgcGo2YXl_66B1nU6zvxgyot8y_CR2wcNTGeDvRLCow130_provenance.
- NP676829.RADgcGo2YXl_66B1nU6zvxgyot8y_CR2wcNTGeDvRLCow130_assertion description "[Based on a total of 5,628 cases and 3,514 controls from JHH, CGEMS, and CAPS, men who carry any combination of 1, 2, 3, and 4 or more of these five risk variants have an estimated OR (95% CI) of 1.41 (1.20-1.67), 1.88 (1.59-2.22), 2.36 (1.95-2.85), and 3.80 (2.77-5.22) for prostate cancer, respectively, compared to men who do not have any of these five risk variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP676829.RADgcGo2YXl_66B1nU6zvxgyot8y_CR2wcNTGeDvRLCow130_provenance.
- NP676829.RADgcGo2YXl_66B1nU6zvxgyot8y_CR2wcNTGeDvRLCow130_assertion evidence source_evidence_literature NP676829.RADgcGo2YXl_66B1nU6zvxgyot8y_CR2wcNTGeDvRLCow130_provenance.
- NP676829.RADgcGo2YXl_66B1nU6zvxgyot8y_CR2wcNTGeDvRLCow130_assertion SIO_000772 18491292 NP676829.RADgcGo2YXl_66B1nU6zvxgyot8y_CR2wcNTGeDvRLCow130_provenance.
- NP676829.RADgcGo2YXl_66B1nU6zvxgyot8y_CR2wcNTGeDvRLCow130_assertion wasDerivedFrom befree-20140225 NP676829.RADgcGo2YXl_66B1nU6zvxgyot8y_CR2wcNTGeDvRLCow130_provenance.
- NP676829.RADgcGo2YXl_66B1nU6zvxgyot8y_CR2wcNTGeDvRLCow130_assertion wasGeneratedBy ECO_0000203 NP676829.RADgcGo2YXl_66B1nU6zvxgyot8y_CR2wcNTGeDvRLCow130_provenance.
- befree-20140225 importedOn "2014-02-25" NP676829.RADgcGo2YXl_66B1nU6zvxgyot8y_CR2wcNTGeDvRLCow130_provenance.