Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP911723.RATGxC-OD6k03Teh3x4ZLaGCK2oEmDMV-rvYZV5gz-XfA130_assertion> ?p ?o ?g. }
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- NP911723.RATGxC-OD6k03Teh3x4ZLaGCK2oEmDMV-rvYZV5gz-XfA130_assertion type Assertion NP911723.RATGxC-OD6k03Teh3x4ZLaGCK2oEmDMV-rvYZV5gz-XfA130_head.
- NP911723.RATGxC-OD6k03Teh3x4ZLaGCK2oEmDMV-rvYZV5gz-XfA130_assertion description "[We identified genetic associations between Beh�et's disease and single-nucleotide polymorphisms (SNPs) in KIAA1529, CPVL, LOC100129342, UBASH3B, and UBAC2 (odds ratio = 2.04, 2.26, 1.84, 1.71, and 1.61, respectively; P value = 4.2 x 10-5, 1.0 x 10-4, 3.0 x 10-4, 1.5 x 10-3, and 5.8 x 10-3, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP911723.RATGxC-OD6k03Teh3x4ZLaGCK2oEmDMV-rvYZV5gz-XfA130_provenance.
- NP911723.RATGxC-OD6k03Teh3x4ZLaGCK2oEmDMV-rvYZV5gz-XfA130_assertion evidence source_evidence_literature NP911723.RATGxC-OD6k03Teh3x4ZLaGCK2oEmDMV-rvYZV5gz-XfA130_provenance.
- NP911723.RATGxC-OD6k03Teh3x4ZLaGCK2oEmDMV-rvYZV5gz-XfA130_assertion SIO_000772 19442274 NP911723.RATGxC-OD6k03Teh3x4ZLaGCK2oEmDMV-rvYZV5gz-XfA130_provenance.
- NP911723.RATGxC-OD6k03Teh3x4ZLaGCK2oEmDMV-rvYZV5gz-XfA130_assertion wasDerivedFrom befree-20150227 NP911723.RATGxC-OD6k03Teh3x4ZLaGCK2oEmDMV-rvYZV5gz-XfA130_provenance.
- NP911723.RATGxC-OD6k03Teh3x4ZLaGCK2oEmDMV-rvYZV5gz-XfA130_assertion wasGeneratedBy ECO_0000203 NP911723.RATGxC-OD6k03Teh3x4ZLaGCK2oEmDMV-rvYZV5gz-XfA130_provenance.