Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP493984.RA9_Jl6Cdpz5lcT4QBnRQGGFj5aJb-QQG5I0SNEn9jiOk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP493984.RA9_Jl6Cdpz5lcT4QBnRQGGFj5aJb-QQG5I0SNEn9jiOk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP493984.RA9_Jl6Cdpz5lcT4QBnRQGGFj5aJb-QQG5I0SNEn9jiOk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP493984.RA9_Jl6Cdpz5lcT4QBnRQGGFj5aJb-QQG5I0SNEn9jiOk130_provenance.
- NP493984.RA9_Jl6Cdpz5lcT4QBnRQGGFj5aJb-QQG5I0SNEn9jiOk130_assertion description "[We observed an accumulation of rare nonsynonymous variants exclusive to RA cases in IL2RA and IL2RB (burden test: p = 0.007 and p = 0.018, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP493984.RA9_Jl6Cdpz5lcT4QBnRQGGFj5aJb-QQG5I0SNEn9jiOk130_provenance.
- NP493984.RA9_Jl6Cdpz5lcT4QBnRQGGFj5aJb-QQG5I0SNEn9jiOk130_assertion evidence source_evidence_literature NP493984.RA9_Jl6Cdpz5lcT4QBnRQGGFj5aJb-QQG5I0SNEn9jiOk130_provenance.
- NP493984.RA9_Jl6Cdpz5lcT4QBnRQGGFj5aJb-QQG5I0SNEn9jiOk130_assertion SIO_000772 23261300 NP493984.RA9_Jl6Cdpz5lcT4QBnRQGGFj5aJb-QQG5I0SNEn9jiOk130_provenance.
- NP493984.RA9_Jl6Cdpz5lcT4QBnRQGGFj5aJb-QQG5I0SNEn9jiOk130_assertion wasDerivedFrom befree-20150227 NP493984.RA9_Jl6Cdpz5lcT4QBnRQGGFj5aJb-QQG5I0SNEn9jiOk130_provenance.
- NP493984.RA9_Jl6Cdpz5lcT4QBnRQGGFj5aJb-QQG5I0SNEn9jiOk130_assertion wasGeneratedBy ECO_0000203 NP493984.RA9_Jl6Cdpz5lcT4QBnRQGGFj5aJb-QQG5I0SNEn9jiOk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP493984.RA9_Jl6Cdpz5lcT4QBnRQGGFj5aJb-QQG5I0SNEn9jiOk130_provenance.