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- source_evidence_literature type ECO_0000212 NP650581.RACOq59tkPIaqq3ECNIw3Cj9_KlAQpPKGEwRX5_BSaYE0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP650581.RACOq59tkPIaqq3ECNIw3Cj9_KlAQpPKGEwRX5_BSaYE0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP650581.RACOq59tkPIaqq3ECNIw3Cj9_KlAQpPKGEwRX5_BSaYE0130_provenance.
- NP650581.RACOq59tkPIaqq3ECNIw3Cj9_KlAQpPKGEwRX5_BSaYE0130_assertion description "[In humans, typing of the +1239A/C single nucleotide polymorphism (SNP) in the 3UTR of the Opn gene (SPP1) showed that +1239C carriers displayed higher Opn serum levels than +1239A homozygotes and a higher risk of developing autoimmune/lymphoproliferative syndrome, multiple sclerosis, and systemic lupus erythematosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650581.RACOq59tkPIaqq3ECNIw3Cj9_KlAQpPKGEwRX5_BSaYE0130_provenance.
- NP650581.RACOq59tkPIaqq3ECNIw3Cj9_KlAQpPKGEwRX5_BSaYE0130_assertion evidence source_evidence_literature NP650581.RACOq59tkPIaqq3ECNIw3Cj9_KlAQpPKGEwRX5_BSaYE0130_provenance.
- NP650581.RACOq59tkPIaqq3ECNIw3Cj9_KlAQpPKGEwRX5_BSaYE0130_assertion SIO_000772 20378012 NP650581.RACOq59tkPIaqq3ECNIw3Cj9_KlAQpPKGEwRX5_BSaYE0130_provenance.
- NP650581.RACOq59tkPIaqq3ECNIw3Cj9_KlAQpPKGEwRX5_BSaYE0130_assertion wasDerivedFrom befree-20140225 NP650581.RACOq59tkPIaqq3ECNIw3Cj9_KlAQpPKGEwRX5_BSaYE0130_provenance.
- NP650581.RACOq59tkPIaqq3ECNIw3Cj9_KlAQpPKGEwRX5_BSaYE0130_assertion wasGeneratedBy ECO_0000203 NP650581.RACOq59tkPIaqq3ECNIw3Cj9_KlAQpPKGEwRX5_BSaYE0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP650581.RACOq59tkPIaqq3ECNIw3Cj9_KlAQpPKGEwRX5_BSaYE0130_provenance.