| Id |
Subject |
Object |
Predicate |
Lexical cue |
mondo_id |
| T1 |
69-98 |
DiseaseOrPhenotypicFeature |
denotes |
congenital muscular dystrophy |
0019950 |
| T2 |
114-139 |
DiseaseOrPhenotypicFeature |
denotes |
laminin alpha2 deficiency |
0011925 |
| T3 |
194-225 |
DiseaseOrPhenotypicFeature |
denotes |
congenital muscular dystrophies |
0019950 |
| T4 |
227-230 |
DiseaseOrPhenotypicFeature |
denotes |
CMD |
0007251|0007397|0019950|0044875 |
| T8 |
441-459 |
DiseaseOrPhenotypicFeature |
denotes |
mental retardation |
0001071 |
| T9 |
496-499 |
DiseaseOrPhenotypicFeature |
denotes |
CMD |
0007251|0007397|0019950|0044875 |
| T13 |
500-509 |
DiseaseOrPhenotypicFeature |
denotes |
syndromes |
0002254 |
| T14 |
546-549 |
DiseaseOrPhenotypicFeature |
denotes |
CMD |
0007251|0007397|0019950|0044875 |
| T18 |
577-582 |
DiseaseOrPhenotypicFeature |
denotes |
MDC1A |
0011925 |
| T19 |
745-748 |
DiseaseOrPhenotypicFeature |
denotes |
CMD |
0007251|0007397|0019950|0044875 |
| T23 |
749-758 |
DiseaseOrPhenotypicFeature |
denotes |
syndromes |
0002254 |
| T24 |
770-775 |
DiseaseOrPhenotypicFeature |
denotes |
MDC1B |
0011486 |
| T25 |
822-846 |
DiseaseOrPhenotypicFeature |
denotes |
muscle-eye-brain disease |
0018939 |
| T26 |
848-851 |
DiseaseOrPhenotypicFeature |
denotes |
MEB |
0018939 |
| T27 |
866-869 |
DiseaseOrPhenotypicFeature |
denotes |
CMD |
0007251|0007397|0019950|0044875 |
| T31 |
871-875 |
DiseaseOrPhenotypicFeature |
denotes |
FCMD |
0009678|0023204 |
| T33 |
923-927 |
DiseaseOrPhenotypicFeature |
denotes |
FCMD |
0009678|0023204 |
| T35 |
1362-1365 |
DiseaseOrPhenotypicFeature |
denotes |
CMD |
0007251|0007397|0019950|0044875 |
| T39 |
1471-1489 |
DiseaseOrPhenotypicFeature |
denotes |
muscle hypertrophy |
0013598 |
| T40 |
1948-1953 |
DiseaseOrPhenotypicFeature |
denotes |
MDC1C |
0011688 |
