Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP922722.RAngoUDyk2RnwscP-EGSTPfhsCDrTFFBQFpsJWk2mHUgk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP922722.RAngoUDyk2RnwscP-EGSTPfhsCDrTFFBQFpsJWk2mHUgk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP922722.RAngoUDyk2RnwscP-EGSTPfhsCDrTFFBQFpsJWk2mHUgk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP922722.RAngoUDyk2RnwscP-EGSTPfhsCDrTFFBQFpsJWk2mHUgk130_provenance.
- NP922722.RAngoUDyk2RnwscP-EGSTPfhsCDrTFFBQFpsJWk2mHUgk130_assertion description "[No significant differences in allele or genotype frequencies for the NOS2A promoter CCTTT repeat microsatellite and NOS3 gene polymorphisms between RA patients with or without CV events were found.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP922722.RAngoUDyk2RnwscP-EGSTPfhsCDrTFFBQFpsJWk2mHUgk130_provenance.
- NP922722.RAngoUDyk2RnwscP-EGSTPfhsCDrTFFBQFpsJWk2mHUgk130_assertion evidence source_evidence_literature NP922722.RAngoUDyk2RnwscP-EGSTPfhsCDrTFFBQFpsJWk2mHUgk130_provenance.
- NP922722.RAngoUDyk2RnwscP-EGSTPfhsCDrTFFBQFpsJWk2mHUgk130_assertion SIO_000772 19327239 NP922722.RAngoUDyk2RnwscP-EGSTPfhsCDrTFFBQFpsJWk2mHUgk130_provenance.
- NP922722.RAngoUDyk2RnwscP-EGSTPfhsCDrTFFBQFpsJWk2mHUgk130_assertion wasDerivedFrom befree-20140225 NP922722.RAngoUDyk2RnwscP-EGSTPfhsCDrTFFBQFpsJWk2mHUgk130_provenance.
- NP922722.RAngoUDyk2RnwscP-EGSTPfhsCDrTFFBQFpsJWk2mHUgk130_assertion wasGeneratedBy ECO_0000203 NP922722.RAngoUDyk2RnwscP-EGSTPfhsCDrTFFBQFpsJWk2mHUgk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP922722.RAngoUDyk2RnwscP-EGSTPfhsCDrTFFBQFpsJWk2mHUgk130_provenance.