| Id |
Subject |
Object |
Predicate |
Lexical cue |
#label |
ID: |
| T25151 |
75-83 |
GeneOrGeneProduct |
denotes |
homeobox |
|
|
| T71873 |
85-88 |
GeneOrGeneProduct |
denotes |
ARX |
|
|
| T98251 |
96-99 |
GeneOrGeneProduct |
denotes |
ARX |
|
|
| T24257 |
138-143 |
OrganismTaxon |
denotes |
human |
|
|
| T1 |
193-206 |
DiseaseOrPhenotypicFeature |
denotes |
malformations |
DISEASE |
|
| T2 |
224-247 |
DiseaseOrPhenotypicFeature |
denotes |
intellectual disability |
D008607 |
|
| T3 |
249-251 |
DiseaseOrPhenotypicFeature |
denotes |
ID |
D008607 |
|
| T24667 |
254-257 |
GeneOrGeneProduct |
denotes |
ARX |
|
|
| T5 |
263-283 |
GeneOrGeneProduct |
denotes |
transcription factor |
|
|
| T10749 |
324-335 |
ChemicalEntity |
denotes |
polyalanine |
|
ChemicalEntity |
| T29393 |
337-339 |
ChemicalEntity |
denotes |
pA |
|
ChemicalEntity |
| T4 |
474-476 |
DiseaseOrPhenotypicFeature |
denotes |
ID |
D008607 |
|
| T6 |
509-512 |
GeneOrGeneProduct |
denotes |
ARX |
|
|
| T18043 |
524-532 |
SequenceVariant |
denotes |
c.304ins |
|
|
| T19110 |
563-575 |
SequenceVariant |
denotes |
c.429_452dup |
|
|
| T7 |
660-663 |
GeneOrGeneProduct |
denotes |
ARX |
|
|
| T8 |
687-695 |
GeneOrGeneProduct |
denotes |
stranded |
|
|
| T9 |
847-850 |
GeneOrGeneProduct |
denotes |
ARX |
|
|
| T10 |
1134-1145 |
GeneOrGeneProduct |
denotes |
homeodomain |
|
|
| T54574 |
1147-1156 |
SequenceVariant |
denotes |
c.1074G>T |
|
|
| T11 |
1197-1200 |
GeneOrGeneProduct |
denotes |
ARX |
|
|
| T52764 |
1250-1258 |
OrganismTaxon |
denotes |
patients |
|
|
| T12 |
1375-1387 |
GeneOrGeneProduct |
denotes |
ARX proteins |
|
|
| T14 |
1595-1606 |
GeneOrGeneProduct |
denotes |
homeodomain |
|
|
