PubMed:20367798 JSONTXT 6 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
20367798-4#82#87#gene149233 616-621 gene149233 denotes IL23R
20367798-4#150#169#diseaseC0004763 684-703 diseaseC0004763 denotes Barrett's esophagus
20367798-0#20#40#diseaseC0859976 1028-1390 diseaseC0859976 denotes iagnosed on the basis of clinical, radiographic, endoscopic, and manometric criteria. All samples were genotyped for the IL23R Arg381Gln polymorphism using TaqMan technology. KEY RESULTS: The minor allele of the Arg381Gln polymorphism was significantly increased in patients compared with healthy controls (OR = 1.46, 95% CI = 1.01-2.11, P = 0.036). This associa
20367798-0#45#50#gene149233 1484-1572 gene149233 denotes I = 1.29-4.16, P = 0.002). CONCLUSIONS & INFERENCES: Our results suggest a role of IL23R
45#50#gene14923320#40#diseaseC0859976 20367798-0#45#50#gene149233 20367798-0#20#40#diseaseC0859976 associated_with "I = 1.29-4.16, P = 0.002). CONCLUSIONS & INFERENCES: Our results suggest a role of IL23R","iagnosed on the basis of clinical, radiographic, endoscopic, and manometric criteria. All samples were genotyped for the IL23R Arg381Gln polymorphism using TaqMan technology. KEY RESULTS: The minor allele of the Arg381Gln polymorphism was significantly increased in patients compared with healthy controls (OR = 1.46, 95% CI = 1.01-2.11, P = 0.036). This associa"
82#87#gene149233150#169#diseaseC0004763 20367798-4#82#87#gene149233 20367798-4#150#169#diseaseC0004763 associated_with IL23R,Barrett's esophagus