Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP618449.RAY8-erco6PdNCtPryipNfDEYI3cmqNcrhtQy0oXVkEKI130_assertion> ?p ?o ?g. }
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- NP618449.RAY8-erco6PdNCtPryipNfDEYI3cmqNcrhtQy0oXVkEKI130_assertion type Assertion NP618449.RAY8-erco6PdNCtPryipNfDEYI3cmqNcrhtQy0oXVkEKI130_head.
- NP618449.RAY8-erco6PdNCtPryipNfDEYI3cmqNcrhtQy0oXVkEKI130_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." NP618449.RAY8-erco6PdNCtPryipNfDEYI3cmqNcrhtQy0oXVkEKI130_provenance.
- NP618449.RAY8-erco6PdNCtPryipNfDEYI3cmqNcrhtQy0oXVkEKI130_assertion evidence source_evidence_literature NP618449.RAY8-erco6PdNCtPryipNfDEYI3cmqNcrhtQy0oXVkEKI130_provenance.
- NP618449.RAY8-erco6PdNCtPryipNfDEYI3cmqNcrhtQy0oXVkEKI130_assertion SIO_000772 17610319 NP618449.RAY8-erco6PdNCtPryipNfDEYI3cmqNcrhtQy0oXVkEKI130_provenance.
- NP618449.RAY8-erco6PdNCtPryipNfDEYI3cmqNcrhtQy0oXVkEKI130_assertion wasDerivedFrom befree-2016 NP618449.RAY8-erco6PdNCtPryipNfDEYI3cmqNcrhtQy0oXVkEKI130_provenance.
- NP618449.RAY8-erco6PdNCtPryipNfDEYI3cmqNcrhtQy0oXVkEKI130_assertion wasGeneratedBy ECO_0000203 NP618449.RAY8-erco6PdNCtPryipNfDEYI3cmqNcrhtQy0oXVkEKI130_provenance.