Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP551076.RAF9uXvigCMBn1qPB4J20-_Fs6Ox80cIlsx_qWWR5bRUg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP551076.RAF9uXvigCMBn1qPB4J20-_Fs6Ox80cIlsx_qWWR5bRUg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP551076.RAF9uXvigCMBn1qPB4J20-_Fs6Ox80cIlsx_qWWR5bRUg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP551076.RAF9uXvigCMBn1qPB4J20-_Fs6Ox80cIlsx_qWWR5bRUg130_provenance.
- NP551076.RAF9uXvigCMBn1qPB4J20-_Fs6Ox80cIlsx_qWWR5bRUg130_assertion description "[In addition, the frequency of IKBLp*01, but not that of other -63T-bearing alleles, was increased in the patients with RA (73.3% vs 58.1%, giving an odds ratio of 1.99), suggesting that the susceptibility to RA was conferred not by -63T alone but by combination of single nucleotide polymorphisms in the NFKBIL1 promoter.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP551076.RAF9uXvigCMBn1qPB4J20-_Fs6Ox80cIlsx_qWWR5bRUg130_provenance.
- NP551076.RAF9uXvigCMBn1qPB4J20-_Fs6Ox80cIlsx_qWWR5bRUg130_assertion evidence source_evidence_literature NP551076.RAF9uXvigCMBn1qPB4J20-_Fs6Ox80cIlsx_qWWR5bRUg130_provenance.
- NP551076.RAF9uXvigCMBn1qPB4J20-_Fs6Ox80cIlsx_qWWR5bRUg130_assertion SIO_000772 16720219 NP551076.RAF9uXvigCMBn1qPB4J20-_Fs6Ox80cIlsx_qWWR5bRUg130_provenance.
- NP551076.RAF9uXvigCMBn1qPB4J20-_Fs6Ox80cIlsx_qWWR5bRUg130_assertion wasDerivedFrom befree-2016 NP551076.RAF9uXvigCMBn1qPB4J20-_Fs6Ox80cIlsx_qWWR5bRUg130_provenance.
- NP551076.RAF9uXvigCMBn1qPB4J20-_Fs6Ox80cIlsx_qWWR5bRUg130_assertion wasGeneratedBy ECO_0000203 NP551076.RAF9uXvigCMBn1qPB4J20-_Fs6Ox80cIlsx_qWWR5bRUg130_provenance.
- befree-2016 importedOn "2016-02-19" NP551076.RAF9uXvigCMBn1qPB4J20-_Fs6Ox80cIlsx_qWWR5bRUg130_provenance.