Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP428498.RA4pYX93AKB6EwpPMhwUBvovCVH3FWIRx0XkzGsnOg7Eo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP428498.RA4pYX93AKB6EwpPMhwUBvovCVH3FWIRx0XkzGsnOg7Eo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP428498.RA4pYX93AKB6EwpPMhwUBvovCVH3FWIRx0XkzGsnOg7Eo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP428498.RA4pYX93AKB6EwpPMhwUBvovCVH3FWIRx0XkzGsnOg7Eo130_provenance.
- NP428498.RA4pYX93AKB6EwpPMhwUBvovCVH3FWIRx0XkzGsnOg7Eo130_assertion description "[The frequency of the minor SEEK1(T) allele in subjects with PsA and controls was 48.5% and 32.4%, respectively (odds ratio (OR) = 2.0; p = 0.017), in the Newfoundland population and 46.5% and 38.0%, respectively (OR = 1.4; p = 0.16), in the Ontario population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428498.RA4pYX93AKB6EwpPMhwUBvovCVH3FWIRx0XkzGsnOg7Eo130_provenance.
- NP428498.RA4pYX93AKB6EwpPMhwUBvovCVH3FWIRx0XkzGsnOg7Eo130_assertion evidence source_evidence_literature NP428498.RA4pYX93AKB6EwpPMhwUBvovCVH3FWIRx0XkzGsnOg7Eo130_provenance.
- NP428498.RA4pYX93AKB6EwpPMhwUBvovCVH3FWIRx0XkzGsnOg7Eo130_assertion SIO_000772 15708881 NP428498.RA4pYX93AKB6EwpPMhwUBvovCVH3FWIRx0XkzGsnOg7Eo130_provenance.
- NP428498.RA4pYX93AKB6EwpPMhwUBvovCVH3FWIRx0XkzGsnOg7Eo130_assertion wasDerivedFrom befree-20140225 NP428498.RA4pYX93AKB6EwpPMhwUBvovCVH3FWIRx0XkzGsnOg7Eo130_provenance.
- NP428498.RA4pYX93AKB6EwpPMhwUBvovCVH3FWIRx0XkzGsnOg7Eo130_assertion wasGeneratedBy ECO_0000203 NP428498.RA4pYX93AKB6EwpPMhwUBvovCVH3FWIRx0XkzGsnOg7Eo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP428498.RA4pYX93AKB6EwpPMhwUBvovCVH3FWIRx0XkzGsnOg7Eo130_provenance.