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 |