Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP968683.RAeGmHshvQ90h1a9_Hp9Glrb0RTiPuI-7Orwzp9NYSGiM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP968683.RAeGmHshvQ90h1a9_Hp9Glrb0RTiPuI-7Orwzp9NYSGiM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP968683.RAeGmHshvQ90h1a9_Hp9Glrb0RTiPuI-7Orwzp9NYSGiM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP968683.RAeGmHshvQ90h1a9_Hp9Glrb0RTiPuI-7Orwzp9NYSGiM130_provenance.
- NP968683.RAeGmHshvQ90h1a9_Hp9Glrb0RTiPuI-7Orwzp9NYSGiM130_assertion description "[In the overall populations, there was a marked association between D allele or DD genotype and SLE susceptibility (D: OR 1.29, 95% CI 1.04-1.58, p = 0.02; DD: OR 1.60, 95% CI 1.17-2.19, p = 0.003), and DD homozygous was associated with LN risk (OR 2.78, 95% CI 1.26-6.11, p = 0.01).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP968683.RAeGmHshvQ90h1a9_Hp9Glrb0RTiPuI-7Orwzp9NYSGiM130_provenance.
- NP968683.RAeGmHshvQ90h1a9_Hp9Glrb0RTiPuI-7Orwzp9NYSGiM130_assertion evidence source_evidence_literature NP968683.RAeGmHshvQ90h1a9_Hp9Glrb0RTiPuI-7Orwzp9NYSGiM130_provenance.
- NP968683.RAeGmHshvQ90h1a9_Hp9Glrb0RTiPuI-7Orwzp9NYSGiM130_assertion SIO_000772 22337243 NP968683.RAeGmHshvQ90h1a9_Hp9Glrb0RTiPuI-7Orwzp9NYSGiM130_provenance.
- NP968683.RAeGmHshvQ90h1a9_Hp9Glrb0RTiPuI-7Orwzp9NYSGiM130_assertion wasDerivedFrom befree-20150227 NP968683.RAeGmHshvQ90h1a9_Hp9Glrb0RTiPuI-7Orwzp9NYSGiM130_provenance.
- NP968683.RAeGmHshvQ90h1a9_Hp9Glrb0RTiPuI-7Orwzp9NYSGiM130_assertion wasGeneratedBy ECO_0000203 NP968683.RAeGmHshvQ90h1a9_Hp9Glrb0RTiPuI-7Orwzp9NYSGiM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP968683.RAeGmHshvQ90h1a9_Hp9Glrb0RTiPuI-7Orwzp9NYSGiM130_provenance.