Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP866199.RA-xMND9P4HjuMSerKJfhOOU8jSy3rr3u3d8-OmXusNwM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP866199.RA-xMND9P4HjuMSerKJfhOOU8jSy3rr3u3d8-OmXusNwM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP866199.RA-xMND9P4HjuMSerKJfhOOU8jSy3rr3u3d8-OmXusNwM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP866199.RA-xMND9P4HjuMSerKJfhOOU8jSy3rr3u3d8-OmXusNwM130_provenance.
- NP866199.RA-xMND9P4HjuMSerKJfhOOU8jSy3rr3u3d8-OmXusNwM130_assertion description "[The rs1229984 (ADH1B), rs1573496 (ADH7) and rs441 (ALDH2) polymorphisms were not associated with CRC risk overall in Western-European populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP866199.RA-xMND9P4HjuMSerKJfhOOU8jSy3rr3u3d8-OmXusNwM130_provenance.
- NP866199.RA-xMND9P4HjuMSerKJfhOOU8jSy3rr3u3d8-OmXusNwM130_assertion evidence source_evidence_literature NP866199.RA-xMND9P4HjuMSerKJfhOOU8jSy3rr3u3d8-OmXusNwM130_provenance.
- NP866199.RA-xMND9P4HjuMSerKJfhOOU8jSy3rr3u3d8-OmXusNwM130_assertion SIO_000772 23149980 NP866199.RA-xMND9P4HjuMSerKJfhOOU8jSy3rr3u3d8-OmXusNwM130_provenance.
- NP866199.RA-xMND9P4HjuMSerKJfhOOU8jSy3rr3u3d8-OmXusNwM130_assertion wasDerivedFrom befree-20140225 NP866199.RA-xMND9P4HjuMSerKJfhOOU8jSy3rr3u3d8-OmXusNwM130_provenance.
- NP866199.RA-xMND9P4HjuMSerKJfhOOU8jSy3rr3u3d8-OmXusNwM130_assertion wasGeneratedBy ECO_0000203 NP866199.RA-xMND9P4HjuMSerKJfhOOU8jSy3rr3u3d8-OmXusNwM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP866199.RA-xMND9P4HjuMSerKJfhOOU8jSy3rr3u3d8-OmXusNwM130_provenance.