Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP115903.RAKvjOJR-U4knQ71T2mRlMXqrhJByp1vNBQf32mRq0mtY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP115903.RAKvjOJR-U4knQ71T2mRlMXqrhJByp1vNBQf32mRq0mtY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP115903.RAKvjOJR-U4knQ71T2mRlMXqrhJByp1vNBQf32mRq0mtY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP115903.RAKvjOJR-U4knQ71T2mRlMXqrhJByp1vNBQf32mRq0mtY130_provenance.
- NP115903.RAKvjOJR-U4knQ71T2mRlMXqrhJByp1vNBQf32mRq0mtY130_assertion description "[This study provides more stable OR estimates for PCa risk-associated SNPs, which is an important baseline for the effect of these SNPs in risk prediction. These SNPs explain a considerable proportion of genetic variance, however, the majority of genetic v]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP115903.RAKvjOJR-U4knQ71T2mRlMXqrhJByp1vNBQf32mRq0mtY130_provenance.
- NP115903.RAKvjOJR-U4knQ71T2mRlMXqrhJByp1vNBQf32mRq0mtY130_assertion evidence source_evidence_literature NP115903.RAKvjOJR-U4knQ71T2mRlMXqrhJByp1vNBQf32mRq0mtY130_provenance.
- NP115903.RAKvjOJR-U4knQ71T2mRlMXqrhJByp1vNBQf32mRq0mtY130_assertion SIO_000772 20564319 NP115903.RAKvjOJR-U4knQ71T2mRlMXqrhJByp1vNBQf32mRq0mtY130_provenance.
- NP115903.RAKvjOJR-U4knQ71T2mRlMXqrhJByp1vNBQf32mRq0mtY130_assertion wasDerivedFrom gad-20150221 NP115903.RAKvjOJR-U4knQ71T2mRlMXqrhJByp1vNBQf32mRq0mtY130_provenance.
- NP115903.RAKvjOJR-U4knQ71T2mRlMXqrhJByp1vNBQf32mRq0mtY130_assertion wasGeneratedBy ECO_0000203 NP115903.RAKvjOJR-U4knQ71T2mRlMXqrhJByp1vNBQf32mRq0mtY130_provenance.
- gad-20150221 importedOn "2015-02-21" NP115903.RAKvjOJR-U4knQ71T2mRlMXqrhJByp1vNBQf32mRq0mtY130_provenance.