Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP590459.RAAEmYuaIdDjAQSec97kLX-ePEpP66hO72RRMTjlTSzXE130_assertion> ?p ?o ?g. }
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- NP590459.RAAEmYuaIdDjAQSec97kLX-ePEpP66hO72RRMTjlTSzXE130_assertion type Assertion NP590459.RAAEmYuaIdDjAQSec97kLX-ePEpP66hO72RRMTjlTSzXE130_head.
- NP590459.RAAEmYuaIdDjAQSec97kLX-ePEpP66hO72RRMTjlTSzXE130_assertion description "[We replicated these findings by genotyping the most associated GD SNP, rs2268458, in a separate UK Caucasian cohort of 1,366 AITD cases and 1,061 controls (GD, P=2 x 10(-6), OR 1.3; AIH, P=NS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP590459.RAAEmYuaIdDjAQSec97kLX-ePEpP66hO72RRMTjlTSzXE130_provenance.
- NP590459.RAAEmYuaIdDjAQSec97kLX-ePEpP66hO72RRMTjlTSzXE130_assertion evidence source_evidence_literature NP590459.RAAEmYuaIdDjAQSec97kLX-ePEpP66hO72RRMTjlTSzXE130_provenance.
- NP590459.RAAEmYuaIdDjAQSec97kLX-ePEpP66hO72RRMTjlTSzXE130_assertion SIO_000772 16106256 NP590459.RAAEmYuaIdDjAQSec97kLX-ePEpP66hO72RRMTjlTSzXE130_provenance.
- NP590459.RAAEmYuaIdDjAQSec97kLX-ePEpP66hO72RRMTjlTSzXE130_assertion wasDerivedFrom befree-20140225 NP590459.RAAEmYuaIdDjAQSec97kLX-ePEpP66hO72RRMTjlTSzXE130_provenance.
- NP590459.RAAEmYuaIdDjAQSec97kLX-ePEpP66hO72RRMTjlTSzXE130_assertion wasGeneratedBy ECO_0000203 NP590459.RAAEmYuaIdDjAQSec97kLX-ePEpP66hO72RRMTjlTSzXE130_provenance.