Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1213012.RAYvgN7hIG3JQl5wY0xo-ro6rVHU2geYcS9H_x2_9ghi0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1213012.RAYvgN7hIG3JQl5wY0xo-ro6rVHU2geYcS9H_x2_9ghi0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1213012.RAYvgN7hIG3JQl5wY0xo-ro6rVHU2geYcS9H_x2_9ghi0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1213012.RAYvgN7hIG3JQl5wY0xo-ro6rVHU2geYcS9H_x2_9ghi0130_provenance.
- NP1213012.RAYvgN7hIG3JQl5wY0xo-ro6rVHU2geYcS9H_x2_9ghi0130_assertion description "[Our finding showed an association between SOD1 DEL/DEL (9% vs. 2.5%) and INS/DEL genotypes and risk of CVD and these genotypes increased the susceptibility to CVD (OR=2.096, 95% CI: 1.336-3.286, P= 0.001 for the INS/DEL genotype; OR=4.811, 95% CI: 1.734-13.346, P= 0.003 for the DEL/DEL genotype).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1213012.RAYvgN7hIG3JQl5wY0xo-ro6rVHU2geYcS9H_x2_9ghi0130_provenance.
- NP1213012.RAYvgN7hIG3JQl5wY0xo-ro6rVHU2geYcS9H_x2_9ghi0130_assertion evidence source_evidence_literature NP1213012.RAYvgN7hIG3JQl5wY0xo-ro6rVHU2geYcS9H_x2_9ghi0130_provenance.
- NP1213012.RAYvgN7hIG3JQl5wY0xo-ro6rVHU2geYcS9H_x2_9ghi0130_assertion SIO_000772 25149881 NP1213012.RAYvgN7hIG3JQl5wY0xo-ro6rVHU2geYcS9H_x2_9ghi0130_provenance.
- NP1213012.RAYvgN7hIG3JQl5wY0xo-ro6rVHU2geYcS9H_x2_9ghi0130_assertion wasDerivedFrom befree-2016 NP1213012.RAYvgN7hIG3JQl5wY0xo-ro6rVHU2geYcS9H_x2_9ghi0130_provenance.
- NP1213012.RAYvgN7hIG3JQl5wY0xo-ro6rVHU2geYcS9H_x2_9ghi0130_assertion wasGeneratedBy ECO_0000203 NP1213012.RAYvgN7hIG3JQl5wY0xo-ro6rVHU2geYcS9H_x2_9ghi0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1213012.RAYvgN7hIG3JQl5wY0xo-ro6rVHU2geYcS9H_x2_9ghi0130_provenance.