Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP772708.RA4qw3xaCuHLst6nk1ms9Gc900rfASZEvg0vVeIzZOqTE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP772708.RA4qw3xaCuHLst6nk1ms9Gc900rfASZEvg0vVeIzZOqTE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP772708.RA4qw3xaCuHLst6nk1ms9Gc900rfASZEvg0vVeIzZOqTE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP772708.RA4qw3xaCuHLst6nk1ms9Gc900rfASZEvg0vVeIzZOqTE130_provenance.
- NP772708.RA4qw3xaCuHLst6nk1ms9Gc900rfASZEvg0vVeIzZOqTE130_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." NP772708.RA4qw3xaCuHLst6nk1ms9Gc900rfASZEvg0vVeIzZOqTE130_provenance.
- NP772708.RA4qw3xaCuHLst6nk1ms9Gc900rfASZEvg0vVeIzZOqTE130_assertion evidence source_evidence_literature NP772708.RA4qw3xaCuHLst6nk1ms9Gc900rfASZEvg0vVeIzZOqTE130_provenance.
- NP772708.RA4qw3xaCuHLst6nk1ms9Gc900rfASZEvg0vVeIzZOqTE130_assertion SIO_000772 21521299 NP772708.RA4qw3xaCuHLst6nk1ms9Gc900rfASZEvg0vVeIzZOqTE130_provenance.
- NP772708.RA4qw3xaCuHLst6nk1ms9Gc900rfASZEvg0vVeIzZOqTE130_assertion wasDerivedFrom befree-20140225 NP772708.RA4qw3xaCuHLst6nk1ms9Gc900rfASZEvg0vVeIzZOqTE130_provenance.
- NP772708.RA4qw3xaCuHLst6nk1ms9Gc900rfASZEvg0vVeIzZOqTE130_assertion wasGeneratedBy ECO_0000203 NP772708.RA4qw3xaCuHLst6nk1ms9Gc900rfASZEvg0vVeIzZOqTE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP772708.RA4qw3xaCuHLst6nk1ms9Gc900rfASZEvg0vVeIzZOqTE130_provenance.