Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1213027.RA6ILtMQ4T2ZffBnWW4tI2J-eHRN6xVrJLF5AcFtrwJHk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1213027.RA6ILtMQ4T2ZffBnWW4tI2J-eHRN6xVrJLF5AcFtrwJHk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1213027.RA6ILtMQ4T2ZffBnWW4tI2J-eHRN6xVrJLF5AcFtrwJHk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1213027.RA6ILtMQ4T2ZffBnWW4tI2J-eHRN6xVrJLF5AcFtrwJHk130_provenance.
- NP1213027.RA6ILtMQ4T2ZffBnWW4tI2J-eHRN6xVrJLF5AcFtrwJHk130_assertion description "[Among these SNPs, the ITGAV-rs3911238-G/C polymorphism was associated with RA disease activity [remission-to-low and moderate-to-high in codominant model (CC vs.GG: OR=1.53, p=0.041 and allele (C vs. G: OR=1.18, p=0.042)] and presence of anti-CCP (codominant CC vs.GG: OR=2.77, p=0.001, allele C vs. G: OR=1.19,p=0.033).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1213027.RA6ILtMQ4T2ZffBnWW4tI2J-eHRN6xVrJLF5AcFtrwJHk130_provenance.
- NP1213027.RA6ILtMQ4T2ZffBnWW4tI2J-eHRN6xVrJLF5AcFtrwJHk130_assertion evidence source_evidence_literature NP1213027.RA6ILtMQ4T2ZffBnWW4tI2J-eHRN6xVrJLF5AcFtrwJHk130_provenance.
- NP1213027.RA6ILtMQ4T2ZffBnWW4tI2J-eHRN6xVrJLF5AcFtrwJHk130_assertion SIO_000772 25150077 NP1213027.RA6ILtMQ4T2ZffBnWW4tI2J-eHRN6xVrJLF5AcFtrwJHk130_provenance.
- NP1213027.RA6ILtMQ4T2ZffBnWW4tI2J-eHRN6xVrJLF5AcFtrwJHk130_assertion wasDerivedFrom befree-2016 NP1213027.RA6ILtMQ4T2ZffBnWW4tI2J-eHRN6xVrJLF5AcFtrwJHk130_provenance.
- NP1213027.RA6ILtMQ4T2ZffBnWW4tI2J-eHRN6xVrJLF5AcFtrwJHk130_assertion wasGeneratedBy ECO_0000203 NP1213027.RA6ILtMQ4T2ZffBnWW4tI2J-eHRN6xVrJLF5AcFtrwJHk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1213027.RA6ILtMQ4T2ZffBnWW4tI2J-eHRN6xVrJLF5AcFtrwJHk130_provenance.