PubMed:15725589 JSONTXT 11 Projects

Annnotations TAB TSV DIC JSON TextAE-old TextAE

Id Subject Object Predicate Lexical cue
15725589-0#0#34#diseaseC0270952 0-34 diseaseC0270952 denotes Oculopharyngeal muscular dystrophy
15725589-0#40#46#gene8106 40-46 gene8106 denotes PABPN1
15725589-1#48#75#diseaseC3899989 134-161 diseaseC3899989 denotes autosomal dominant disorder
15725589-1#104#125#diseaseC0743319 190-211 diseaseC0743319 denotes progressive dysphagia
15725589-1#130#143#diseaseC0005745 216-229 diseaseC0005745 denotes eyelid ptosis
15725589-1#272#278#gene8106 358-364 gene8106 denotes PABPN1
272#278#gene8106104#125#diseaseC0743319 15725589-1#272#278#gene8106 15725589-1#104#125#diseaseC0743319 associated_with PABPN1,progressive dysphagia
272#278#gene8106130#143#diseaseC0005745 15725589-1#272#278#gene8106 15725589-1#130#143#diseaseC0005745 associated_with PABPN1,eyelid ptosis
272#278#gene810648#75#diseaseC3899989 15725589-1#272#278#gene8106 15725589-1#48#75#diseaseC3899989 associated_with PABPN1,autosomal dominant disorder
40#46#gene81060#34#diseaseC0270952 15725589-0#40#46#gene8106 15725589-0#0#34#diseaseC0270952 associated_with PABPN1,Oculopharyngeal muscular dystrophy