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- source_evidence_literature type ECO_0000212 NP273481.RA5mubtAsUH39DXkTnZmOmaXo3D_cX9lXq3r4iPTfLNgA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP273481.RA5mubtAsUH39DXkTnZmOmaXo3D_cX9lXq3r4iPTfLNgA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP273481.RA5mubtAsUH39DXkTnZmOmaXo3D_cX9lXq3r4iPTfLNgA130_provenance.
- NP273481.RA5mubtAsUH39DXkTnZmOmaXo3D_cX9lXq3r4iPTfLNgA130_assertion description "[SLE patients with the homozygous or compound heterozygous variant genotype (O/O; O, a common designation for variant alleles) had an increased likelihood of mounting autoantibody responses against dsDNA, Ro/SSA, and La/SSB, and were more likely to have a history of renal disease (OR 4.8; 95% CI 0.9-25.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP273481.RA5mubtAsUH39DXkTnZmOmaXo3D_cX9lXq3r4iPTfLNgA130_provenance.
- NP273481.RA5mubtAsUH39DXkTnZmOmaXo3D_cX9lXq3r4iPTfLNgA130_assertion evidence source_evidence_literature NP273481.RA5mubtAsUH39DXkTnZmOmaXo3D_cX9lXq3r4iPTfLNgA130_provenance.
- NP273481.RA5mubtAsUH39DXkTnZmOmaXo3D_cX9lXq3r4iPTfLNgA130_assertion SIO_000772 17610319 NP273481.RA5mubtAsUH39DXkTnZmOmaXo3D_cX9lXq3r4iPTfLNgA130_provenance.
- NP273481.RA5mubtAsUH39DXkTnZmOmaXo3D_cX9lXq3r4iPTfLNgA130_assertion wasDerivedFrom befree-20140225 NP273481.RA5mubtAsUH39DXkTnZmOmaXo3D_cX9lXq3r4iPTfLNgA130_provenance.
- NP273481.RA5mubtAsUH39DXkTnZmOmaXo3D_cX9lXq3r4iPTfLNgA130_assertion wasGeneratedBy ECO_0000203 NP273481.RA5mubtAsUH39DXkTnZmOmaXo3D_cX9lXq3r4iPTfLNgA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP273481.RA5mubtAsUH39DXkTnZmOmaXo3D_cX9lXq3r4iPTfLNgA130_provenance.