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- source_evidence_literature type ECO_0000212 NP618449.RAY8-erco6PdNCtPryipNfDEYI3cmqNcrhtQy0oXVkEKI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP618449.RAY8-erco6PdNCtPryipNfDEYI3cmqNcrhtQy0oXVkEKI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP618449.RAY8-erco6PdNCtPryipNfDEYI3cmqNcrhtQy0oXVkEKI130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP618449.RAY8-erco6PdNCtPryipNfDEYI3cmqNcrhtQy0oXVkEKI130_provenance.