Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP77544.RAB4Cfz42KZd0NBlOJy_YnQykj0A1djuBaTN2DsDKsIRI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP77544.RAB4Cfz42KZd0NBlOJy_YnQykj0A1djuBaTN2DsDKsIRI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP77544.RAB4Cfz42KZd0NBlOJy_YnQykj0A1djuBaTN2DsDKsIRI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP77544.RAB4Cfz42KZd0NBlOJy_YnQykj0A1djuBaTN2DsDKsIRI130_provenance.
- NP77544.RAB4Cfz42KZd0NBlOJy_YnQykj0A1djuBaTN2DsDKsIRI130_assertion description "[FcgammaRIIa genotypes, but not FcgammaRIIIa and FcgammaRIIIb genotypes, were differentially distributed among 107 MG patients as compared to 239 healthy controls (Pz.Lt;0.01), with a relative increase of the FcgammaRIIa-R/R131 genotype (Odds ratio 2.4, 95% confidence interval 1.4-3.9).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP77544.RAB4Cfz42KZd0NBlOJy_YnQykj0A1djuBaTN2DsDKsIRI130_provenance.
- NP77544.RAB4Cfz42KZd0NBlOJy_YnQykj0A1djuBaTN2DsDKsIRI130_assertion evidence source_evidence_literature NP77544.RAB4Cfz42KZd0NBlOJy_YnQykj0A1djuBaTN2DsDKsIRI130_provenance.
- NP77544.RAB4Cfz42KZd0NBlOJy_YnQykj0A1djuBaTN2DsDKsIRI130_assertion SIO_000772 14597109 NP77544.RAB4Cfz42KZd0NBlOJy_YnQykj0A1djuBaTN2DsDKsIRI130_provenance.
- NP77544.RAB4Cfz42KZd0NBlOJy_YnQykj0A1djuBaTN2DsDKsIRI130_assertion wasDerivedFrom gad-20150221 NP77544.RAB4Cfz42KZd0NBlOJy_YnQykj0A1djuBaTN2DsDKsIRI130_provenance.
- NP77544.RAB4Cfz42KZd0NBlOJy_YnQykj0A1djuBaTN2DsDKsIRI130_assertion wasGeneratedBy ECO_0000203 NP77544.RAB4Cfz42KZd0NBlOJy_YnQykj0A1djuBaTN2DsDKsIRI130_provenance.
- gad-20150221 importedOn "2015-02-21" NP77544.RAB4Cfz42KZd0NBlOJy_YnQykj0A1djuBaTN2DsDKsIRI130_provenance.