Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP830711.RAYb6RpFK_WJSQ2GpU9i3e7D6GXosh4vQ2K5bJygh9Q0M130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP830711.RAYb6RpFK_WJSQ2GpU9i3e7D6GXosh4vQ2K5bJygh9Q0M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP830711.RAYb6RpFK_WJSQ2GpU9i3e7D6GXosh4vQ2K5bJygh9Q0M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP830711.RAYb6RpFK_WJSQ2GpU9i3e7D6GXosh4vQ2K5bJygh9Q0M130_provenance.
- NP830711.RAYb6RpFK_WJSQ2GpU9i3e7D6GXosh4vQ2K5bJygh9Q0M130_assertion description "[Compared with homozygotes for the common allele, the odds ratio (OR) [95% CI] for metabolic syndrome was 1.30 [1.03-1.66] (p = 0.03) for APOA5 Trp19 carriers, 0.81 [0.69-0.95] (p = 0.01) for APOA5 -12,238C carriers and 0.84 [0.70-0.99] (p = 0.04) for APOA4 Ser347 carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP830711.RAYb6RpFK_WJSQ2GpU9i3e7D6GXosh4vQ2K5bJygh9Q0M130_provenance.
- NP830711.RAYb6RpFK_WJSQ2GpU9i3e7D6GXosh4vQ2K5bJygh9Q0M130_assertion evidence source_evidence_literature NP830711.RAYb6RpFK_WJSQ2GpU9i3e7D6GXosh4vQ2K5bJygh9Q0M130_provenance.
- NP830711.RAYb6RpFK_WJSQ2GpU9i3e7D6GXosh4vQ2K5bJygh9Q0M130_assertion SIO_000772 18789138 NP830711.RAYb6RpFK_WJSQ2GpU9i3e7D6GXosh4vQ2K5bJygh9Q0M130_provenance.
- NP830711.RAYb6RpFK_WJSQ2GpU9i3e7D6GXosh4vQ2K5bJygh9Q0M130_assertion wasDerivedFrom befree-20140225 NP830711.RAYb6RpFK_WJSQ2GpU9i3e7D6GXosh4vQ2K5bJygh9Q0M130_provenance.
- NP830711.RAYb6RpFK_WJSQ2GpU9i3e7D6GXosh4vQ2K5bJygh9Q0M130_assertion wasGeneratedBy ECO_0000203 NP830711.RAYb6RpFK_WJSQ2GpU9i3e7D6GXosh4vQ2K5bJygh9Q0M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP830711.RAYb6RpFK_WJSQ2GpU9i3e7D6GXosh4vQ2K5bJygh9Q0M130_provenance.