Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP889771.RAZjJXFM8vCkmWllK_V8VI1yqW6ZhFgnqzFDOwwZzzEI0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP889771.RAZjJXFM8vCkmWllK_V8VI1yqW6ZhFgnqzFDOwwZzzEI0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP889771.RAZjJXFM8vCkmWllK_V8VI1yqW6ZhFgnqzFDOwwZzzEI0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP889771.RAZjJXFM8vCkmWllK_V8VI1yqW6ZhFgnqzFDOwwZzzEI0130_provenance.
- NP889771.RAZjJXFM8vCkmWllK_V8VI1yqW6ZhFgnqzFDOwwZzzEI0130_assertion description "[PATIENT AND DESIGN: We genotyped rs763361 in a UK cohort of 326 AAD subjects [183 with associated autoimmune conditions - autoimmune polyendocrinopathy syndrome type-2 (APS2)] and 311 healthy controls, using a Taqman genotyping assay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP889771.RAZjJXFM8vCkmWllK_V8VI1yqW6ZhFgnqzFDOwwZzzEI0130_provenance.
- NP889771.RAZjJXFM8vCkmWllK_V8VI1yqW6ZhFgnqzFDOwwZzzEI0130_assertion evidence source_evidence_literature NP889771.RAZjJXFM8vCkmWllK_V8VI1yqW6ZhFgnqzFDOwwZzzEI0130_provenance.
- NP889771.RAZjJXFM8vCkmWllK_V8VI1yqW6ZhFgnqzFDOwwZzzEI0130_assertion SIO_000772 21521299 NP889771.RAZjJXFM8vCkmWllK_V8VI1yqW6ZhFgnqzFDOwwZzzEI0130_provenance.
- NP889771.RAZjJXFM8vCkmWllK_V8VI1yqW6ZhFgnqzFDOwwZzzEI0130_assertion wasDerivedFrom befree-2016 NP889771.RAZjJXFM8vCkmWllK_V8VI1yqW6ZhFgnqzFDOwwZzzEI0130_provenance.
- NP889771.RAZjJXFM8vCkmWllK_V8VI1yqW6ZhFgnqzFDOwwZzzEI0130_assertion wasGeneratedBy ECO_0000203 NP889771.RAZjJXFM8vCkmWllK_V8VI1yqW6ZhFgnqzFDOwwZzzEI0130_provenance.
- befree-2016 importedOn "2016-02-19" NP889771.RAZjJXFM8vCkmWllK_V8VI1yqW6ZhFgnqzFDOwwZzzEI0130_provenance.