Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP868113.RA8_TKZWoFZcxc-gORvDGFVOYB2hb8dJSxAicwlbF6aTM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP868113.RA8_TKZWoFZcxc-gORvDGFVOYB2hb8dJSxAicwlbF6aTM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP868113.RA8_TKZWoFZcxc-gORvDGFVOYB2hb8dJSxAicwlbF6aTM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP868113.RA8_TKZWoFZcxc-gORvDGFVOYB2hb8dJSxAicwlbF6aTM130_provenance.
- NP868113.RA8_TKZWoFZcxc-gORvDGFVOYB2hb8dJSxAicwlbF6aTM130_assertion description "[Analysis of common TREX1 SNPs (minor allele frequency (MAF)>10%) revealed a relatively common risk haplotype in European SLE patients with neurological manifestations, especially seizures, with a frequency of 58% in lupus cases compared with 45% in normal controls (P=0.0008, OR=1.73, 95% CI=1.25-2.39).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868113.RA8_TKZWoFZcxc-gORvDGFVOYB2hb8dJSxAicwlbF6aTM130_provenance.
- NP868113.RA8_TKZWoFZcxc-gORvDGFVOYB2hb8dJSxAicwlbF6aTM130_assertion evidence source_evidence_literature NP868113.RA8_TKZWoFZcxc-gORvDGFVOYB2hb8dJSxAicwlbF6aTM130_provenance.
- NP868113.RA8_TKZWoFZcxc-gORvDGFVOYB2hb8dJSxAicwlbF6aTM130_assertion SIO_000772 21270825 NP868113.RA8_TKZWoFZcxc-gORvDGFVOYB2hb8dJSxAicwlbF6aTM130_provenance.
- NP868113.RA8_TKZWoFZcxc-gORvDGFVOYB2hb8dJSxAicwlbF6aTM130_assertion wasDerivedFrom befree-2016 NP868113.RA8_TKZWoFZcxc-gORvDGFVOYB2hb8dJSxAicwlbF6aTM130_provenance.
- NP868113.RA8_TKZWoFZcxc-gORvDGFVOYB2hb8dJSxAicwlbF6aTM130_assertion wasGeneratedBy ECO_0000203 NP868113.RA8_TKZWoFZcxc-gORvDGFVOYB2hb8dJSxAicwlbF6aTM130_provenance.
- befree-2016 importedOn "2016-02-19" NP868113.RA8_TKZWoFZcxc-gORvDGFVOYB2hb8dJSxAicwlbF6aTM130_provenance.