Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP713552.RAvBrrD0vk_pphfVhgH4O_3_Y1Ngehu9-_v8GVEg1ga-w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP713552.RAvBrrD0vk_pphfVhgH4O_3_Y1Ngehu9-_v8GVEg1ga-w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP713552.RAvBrrD0vk_pphfVhgH4O_3_Y1Ngehu9-_v8GVEg1ga-w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP713552.RAvBrrD0vk_pphfVhgH4O_3_Y1Ngehu9-_v8GVEg1ga-w130_provenance.
- NP713552.RAvBrrD0vk_pphfVhgH4O_3_Y1Ngehu9-_v8GVEg1ga-w130_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." NP713552.RAvBrrD0vk_pphfVhgH4O_3_Y1Ngehu9-_v8GVEg1ga-w130_provenance.
- NP713552.RAvBrrD0vk_pphfVhgH4O_3_Y1Ngehu9-_v8GVEg1ga-w130_assertion evidence source_evidence_literature NP713552.RAvBrrD0vk_pphfVhgH4O_3_Y1Ngehu9-_v8GVEg1ga-w130_provenance.
- NP713552.RAvBrrD0vk_pphfVhgH4O_3_Y1Ngehu9-_v8GVEg1ga-w130_assertion SIO_000772 17610319 NP713552.RAvBrrD0vk_pphfVhgH4O_3_Y1Ngehu9-_v8GVEg1ga-w130_provenance.
- NP713552.RAvBrrD0vk_pphfVhgH4O_3_Y1Ngehu9-_v8GVEg1ga-w130_assertion wasDerivedFrom befree-20150227 NP713552.RAvBrrD0vk_pphfVhgH4O_3_Y1Ngehu9-_v8GVEg1ga-w130_provenance.
- NP713552.RAvBrrD0vk_pphfVhgH4O_3_Y1Ngehu9-_v8GVEg1ga-w130_assertion wasGeneratedBy ECO_0000203 NP713552.RAvBrrD0vk_pphfVhgH4O_3_Y1Ngehu9-_v8GVEg1ga-w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP713552.RAvBrrD0vk_pphfVhgH4O_3_Y1Ngehu9-_v8GVEg1ga-w130_provenance.