Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP742570.RAax7WTiWy8Qh7A7ogIDUpOtkWlGQE-A4ACCcjEggtpcM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP742570.RAax7WTiWy8Qh7A7ogIDUpOtkWlGQE-A4ACCcjEggtpcM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP742570.RAax7WTiWy8Qh7A7ogIDUpOtkWlGQE-A4ACCcjEggtpcM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP742570.RAax7WTiWy8Qh7A7ogIDUpOtkWlGQE-A4ACCcjEggtpcM130_provenance.
- NP742570.RAax7WTiWy8Qh7A7ogIDUpOtkWlGQE-A4ACCcjEggtpcM130_assertion description "[Adjustment for prevalent and incident diabetes attenuated the association of the TSPAN8 variant (1.06, 0.99-1.13) and the genetic score (1.05, 0.99-1.12 per score tertile) with CHD risk, but not that of the CDKN2A/B variant (1.11, 1.05-1.18).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP742570.RAax7WTiWy8Qh7A7ogIDUpOtkWlGQE-A4ACCcjEggtpcM130_provenance.
- NP742570.RAax7WTiWy8Qh7A7ogIDUpOtkWlGQE-A4ACCcjEggtpcM130_assertion evidence source_evidence_literature NP742570.RAax7WTiWy8Qh7A7ogIDUpOtkWlGQE-A4ACCcjEggtpcM130_provenance.
- NP742570.RAax7WTiWy8Qh7A7ogIDUpOtkWlGQE-A4ACCcjEggtpcM130_assertion SIO_000772 21638130 NP742570.RAax7WTiWy8Qh7A7ogIDUpOtkWlGQE-A4ACCcjEggtpcM130_provenance.
- NP742570.RAax7WTiWy8Qh7A7ogIDUpOtkWlGQE-A4ACCcjEggtpcM130_assertion wasDerivedFrom befree-20150227 NP742570.RAax7WTiWy8Qh7A7ogIDUpOtkWlGQE-A4ACCcjEggtpcM130_provenance.
- NP742570.RAax7WTiWy8Qh7A7ogIDUpOtkWlGQE-A4ACCcjEggtpcM130_assertion wasGeneratedBy ECO_0000203 NP742570.RAax7WTiWy8Qh7A7ogIDUpOtkWlGQE-A4ACCcjEggtpcM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP742570.RAax7WTiWy8Qh7A7ogIDUpOtkWlGQE-A4ACCcjEggtpcM130_provenance.