Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP290706.RAqSGK3PtHDtODiI5rnshXhpwmKHLxsYhIfL5ZC6raf4U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP290706.RAqSGK3PtHDtODiI5rnshXhpwmKHLxsYhIfL5ZC6raf4U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP290706.RAqSGK3PtHDtODiI5rnshXhpwmKHLxsYhIfL5ZC6raf4U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP290706.RAqSGK3PtHDtODiI5rnshXhpwmKHLxsYhIfL5ZC6raf4U130_provenance.
- NP290706.RAqSGK3PtHDtODiI5rnshXhpwmKHLxsYhIfL5ZC6raf4U130_assertion description "[We studied polymorphism of Ala17Thr CTLA4, H60R LMP2, Pro52Thr TSHR, and IL1RN-VNTR in healthy controls (n = 93) and patients with Graves disease (n = 78) using PCR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP290706.RAqSGK3PtHDtODiI5rnshXhpwmKHLxsYhIfL5ZC6raf4U130_provenance.
- NP290706.RAqSGK3PtHDtODiI5rnshXhpwmKHLxsYhIfL5ZC6raf4U130_assertion evidence source_evidence_literature NP290706.RAqSGK3PtHDtODiI5rnshXhpwmKHLxsYhIfL5ZC6raf4U130_provenance.
- NP290706.RAqSGK3PtHDtODiI5rnshXhpwmKHLxsYhIfL5ZC6raf4U130_assertion SIO_000772 10924276 NP290706.RAqSGK3PtHDtODiI5rnshXhpwmKHLxsYhIfL5ZC6raf4U130_provenance.
- NP290706.RAqSGK3PtHDtODiI5rnshXhpwmKHLxsYhIfL5ZC6raf4U130_assertion wasDerivedFrom befree-2016 NP290706.RAqSGK3PtHDtODiI5rnshXhpwmKHLxsYhIfL5ZC6raf4U130_provenance.
- NP290706.RAqSGK3PtHDtODiI5rnshXhpwmKHLxsYhIfL5ZC6raf4U130_assertion wasGeneratedBy ECO_0000203 NP290706.RAqSGK3PtHDtODiI5rnshXhpwmKHLxsYhIfL5ZC6raf4U130_provenance.
- befree-2016 importedOn "2016-02-19" NP290706.RAqSGK3PtHDtODiI5rnshXhpwmKHLxsYhIfL5ZC6raf4U130_provenance.