| Id |
Subject |
Object |
Predicate |
Lexical cue |
#label |
| T1 |
5-13 |
DiseaseOrPhenotypicFeature |
denotes |
monosomy |
D009006 |
| T2 |
23-30 |
DiseaseOrPhenotypicFeature |
denotes |
trisomy |
D014314 |
| T84697 |
112-117 |
GeneOrGeneProduct |
denotes |
PCDH9 |
|
| T3 |
165-184 |
DiseaseOrPhenotypicFeature |
denotes |
auditory neuropathy |
C538268 |
| T1153 |
186-191 |
GeneOrGeneProduct |
denotes |
AUNA1 |
|
| T4 |
333-348 |
DiseaseOrPhenotypicFeature |
denotes |
partial trisomy |
D014314 |
| T5 |
352-360 |
DiseaseOrPhenotypicFeature |
denotes |
monosomy |
D009006 |
| T6 |
698-706 |
DiseaseOrPhenotypicFeature |
denotes |
monosomy |
D009006 |
| T7 |
716-724 |
DiseaseOrPhenotypicFeature |
denotes |
deafness |
D003638 |
| T8 |
726-743 |
DiseaseOrPhenotypicFeature |
denotes |
duodenal stenosis |
C535720 |
| T9 |
763-775 |
DiseaseOrPhenotypicFeature |
denotes |
growth delay |
DISEASE |
| T75283 |
777-786 |
OrganismTaxon |
denotes |
vertebral |
|
| T10 |
827-834 |
DiseaseOrPhenotypicFeature |
denotes |
trisomy |
D014314 |
| T8306 |
885-890 |
GeneOrGeneProduct |
denotes |
AUNA1 |
|
| T11 |
891-899 |
DiseaseOrPhenotypicFeature |
denotes |
deafness |
D003638 |
| T72188 |
941-946 |
GeneOrGeneProduct |
denotes |
PCDH9 |
|
| T16597 |
948-963 |
GeneOrGeneProduct |
denotes |
protocadherin-9 |
|
| T2215 |
978-983 |
GeneOrGeneProduct |
denotes |
PCDH9 |
|
| T12 |
1025-1033 |
DiseaseOrPhenotypicFeature |
denotes |
deafness |
D003638 |
| T90556 |
1119-1124 |
GeneOrGeneProduct |
denotes |
AUNA1 |
|
| T73161 |
1151-1156 |
GeneOrGeneProduct |
denotes |
PCDH9 |
|
| T97445 |
1241-1246 |
GeneOrGeneProduct |
denotes |
AUNA1 |
|
| T48581 |
1265-1273 |
GeneOrGeneProduct |
denotes |
retained |
|
| T47837 |
1312-1319 |
OrganismTaxon |
denotes |
patient |
|
| T38572 |
1360-1365 |
GeneOrGeneProduct |
denotes |
AUNA1 |
|
| T13 |
1366-1374 |
DiseaseOrPhenotypicFeature |
denotes |
deafness |
D003638 |
| T14 |
1413-1421 |
DiseaseOrPhenotypicFeature |
denotes |
deafness |
D003638 |
| T15 |
1438-1446 |
DiseaseOrPhenotypicFeature |
denotes |
monosomy |
D009006 |
| T16 |
1462-1470 |
DiseaseOrPhenotypicFeature |
denotes |
deafness |
D003638 |
| T17 |
1487-1495 |
DiseaseOrPhenotypicFeature |
denotes |
monosomy |
D009006 |
| T50253 |
1776-1781 |
GeneOrGeneProduct |
denotes |
extra |
|
