Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP889998.RAb0EhgAMogGTsNWdhZEdHObqnIcNtdAIVfOMI9TS2B1I130_assertion> ?p ?o ?g. }
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- NP889998.RAb0EhgAMogGTsNWdhZEdHObqnIcNtdAIVfOMI9TS2B1I130_assertion type Assertion NP889998.RAb0EhgAMogGTsNWdhZEdHObqnIcNtdAIVfOMI9TS2B1I130_head.
- NP889998.RAb0EhgAMogGTsNWdhZEdHObqnIcNtdAIVfOMI9TS2B1I130_assertion description "[In addition, two intronic SNPs in LD with the disease haplotype, one in intron 13 (rs2235035) and another in intron 16 (rs1922242), were significantly associated with refractory Crohn (P=0.026, odds ratio (OR) 2.7 and P=0.025, OR 2.8, respectively), as well as with UC (P=0.006, OR 1.8 and P=0.026, OR 1.9, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP889998.RAb0EhgAMogGTsNWdhZEdHObqnIcNtdAIVfOMI9TS2B1I130_provenance.
- NP889998.RAb0EhgAMogGTsNWdhZEdHObqnIcNtdAIVfOMI9TS2B1I130_assertion evidence source_evidence_literature NP889998.RAb0EhgAMogGTsNWdhZEdHObqnIcNtdAIVfOMI9TS2B1I130_provenance.
- NP889998.RAb0EhgAMogGTsNWdhZEdHObqnIcNtdAIVfOMI9TS2B1I130_assertion SIO_000772 15505619 NP889998.RAb0EhgAMogGTsNWdhZEdHObqnIcNtdAIVfOMI9TS2B1I130_provenance.
- NP889998.RAb0EhgAMogGTsNWdhZEdHObqnIcNtdAIVfOMI9TS2B1I130_assertion wasDerivedFrom befree-20140225 NP889998.RAb0EhgAMogGTsNWdhZEdHObqnIcNtdAIVfOMI9TS2B1I130_provenance.
- NP889998.RAb0EhgAMogGTsNWdhZEdHObqnIcNtdAIVfOMI9TS2B1I130_assertion wasGeneratedBy ECO_0000203 NP889998.RAb0EhgAMogGTsNWdhZEdHObqnIcNtdAIVfOMI9TS2B1I130_provenance.