Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP195418.RA5WZdAEZEEu_xJROQDbcJ3USFpic-9a0Sus-2dScTCiM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP195418.RA5WZdAEZEEu_xJROQDbcJ3USFpic-9a0Sus-2dScTCiM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP195418.RA5WZdAEZEEu_xJROQDbcJ3USFpic-9a0Sus-2dScTCiM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP195418.RA5WZdAEZEEu_xJROQDbcJ3USFpic-9a0Sus-2dScTCiM130_provenance.
- NP195418.RA5WZdAEZEEu_xJROQDbcJ3USFpic-9a0Sus-2dScTCiM130_assertion description "[Carrier rates of MEFV gene mutations were 26/103 (25.2%) and 24/103 (23.3%) in the RA and HC groups, respectively (p>0.05, OR: 0.9, 95% CI: 0.48-1.71).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP195418.RA5WZdAEZEEu_xJROQDbcJ3USFpic-9a0Sus-2dScTCiM130_provenance.
- NP195418.RA5WZdAEZEEu_xJROQDbcJ3USFpic-9a0Sus-2dScTCiM130_assertion evidence source_evidence_literature NP195418.RA5WZdAEZEEu_xJROQDbcJ3USFpic-9a0Sus-2dScTCiM130_provenance.
- NP195418.RA5WZdAEZEEu_xJROQDbcJ3USFpic-9a0Sus-2dScTCiM130_assertion SIO_000772 20031469 NP195418.RA5WZdAEZEEu_xJROQDbcJ3USFpic-9a0Sus-2dScTCiM130_provenance.
- NP195418.RA5WZdAEZEEu_xJROQDbcJ3USFpic-9a0Sus-2dScTCiM130_assertion wasDerivedFrom befree-20140225 NP195418.RA5WZdAEZEEu_xJROQDbcJ3USFpic-9a0Sus-2dScTCiM130_provenance.
- NP195418.RA5WZdAEZEEu_xJROQDbcJ3USFpic-9a0Sus-2dScTCiM130_assertion wasGeneratedBy ECO_0000203 NP195418.RA5WZdAEZEEu_xJROQDbcJ3USFpic-9a0Sus-2dScTCiM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP195418.RA5WZdAEZEEu_xJROQDbcJ3USFpic-9a0Sus-2dScTCiM130_provenance.