DisGeNET5_variant_disease Home  

PubMed:20809772 JSONTXT 10 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
20809772-1#33#50#diseaseC0220658 169-186 diseaseC0220658 denotes Pfeiffer syndrome
20809772-1#117#126#geners121918499 253-262 geners121918499 denotes Trp290Cys
117#126#geners12191849933#50#diseaseC0220658 20809772-1#117#126#geners121918499 20809772-1#33#50#diseaseC0220658 associated_with Trp290Cys,Pfeiffer syndrome