Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP863872.RAlAHO1HlzHPbchLVO4Fn6t-zZs-aUPPdZuRQ0mylXm3I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP863872.RAlAHO1HlzHPbchLVO4Fn6t-zZs-aUPPdZuRQ0mylXm3I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP863872.RAlAHO1HlzHPbchLVO4Fn6t-zZs-aUPPdZuRQ0mylXm3I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP863872.RAlAHO1HlzHPbchLVO4Fn6t-zZs-aUPPdZuRQ0mylXm3I130_provenance.
- NP863872.RAlAHO1HlzHPbchLVO4Fn6t-zZs-aUPPdZuRQ0mylXm3I130_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." NP863872.RAlAHO1HlzHPbchLVO4Fn6t-zZs-aUPPdZuRQ0mylXm3I130_provenance.
- NP863872.RAlAHO1HlzHPbchLVO4Fn6t-zZs-aUPPdZuRQ0mylXm3I130_assertion evidence source_evidence_literature NP863872.RAlAHO1HlzHPbchLVO4Fn6t-zZs-aUPPdZuRQ0mylXm3I130_provenance.
- NP863872.RAlAHO1HlzHPbchLVO4Fn6t-zZs-aUPPdZuRQ0mylXm3I130_assertion SIO_000772 21270825 NP863872.RAlAHO1HlzHPbchLVO4Fn6t-zZs-aUPPdZuRQ0mylXm3I130_provenance.
- NP863872.RAlAHO1HlzHPbchLVO4Fn6t-zZs-aUPPdZuRQ0mylXm3I130_assertion wasDerivedFrom befree-20150227 NP863872.RAlAHO1HlzHPbchLVO4Fn6t-zZs-aUPPdZuRQ0mylXm3I130_provenance.
- NP863872.RAlAHO1HlzHPbchLVO4Fn6t-zZs-aUPPdZuRQ0mylXm3I130_assertion wasGeneratedBy ECO_0000203 NP863872.RAlAHO1HlzHPbchLVO4Fn6t-zZs-aUPPdZuRQ0mylXm3I130_provenance.
- befree-20150227 importedOn "2015-02-27" NP863872.RAlAHO1HlzHPbchLVO4Fn6t-zZs-aUPPdZuRQ0mylXm3I130_provenance.