| Id |
Subject |
Object |
Predicate |
Lexical cue |
#label |
ID: |
| T10251 |
26-30 |
GeneOrGeneProduct |
denotes |
WFS1 |
|
|
| T27297 |
68-76 |
OrganismTaxon |
denotes |
patients |
|
|
| T1 |
82-89 |
ChemicalEntity |
denotes |
Wolfram |
|
D014414 |
| T66029 |
82-98 |
DiseaseOrPhenotypicFeature |
denotes |
Wolfram syndrome |
D014929 |
|
| T2 |
100-107 |
ChemicalEntity |
denotes |
Wolfram |
|
D014414 |
| T2594 |
100-116 |
DiseaseOrPhenotypicFeature |
denotes |
Wolfram syndrome |
D014929 |
|
| T87043 |
118-121 |
DiseaseOrPhenotypicFeature |
denotes |
WFS |
D014929 |
|
| T86911 |
129-157 |
DiseaseOrPhenotypicFeature |
denotes |
autosomal recessive disorder |
DISEASE |
|
| T5 |
187-204 |
DiseaseOrPhenotypicFeature |
denotes |
diabetes mellitus |
D003920 |
|
| T6 |
218-231 |
DiseaseOrPhenotypicFeature |
denotes |
optic atrophy |
D009896 |
|
| T7 |
247-255 |
DiseaseOrPhenotypicFeature |
denotes |
deafness |
D003638 |
|
| T8 |
260-278 |
DiseaseOrPhenotypicFeature |
denotes |
diabetes insipidus |
D003919 |
|
| T9 |
315-340 |
DiseaseOrPhenotypicFeature |
denotes |
renal tract abnormalities |
DISEASE |
|
| T10 |
367-378 |
DiseaseOrPhenotypicFeature |
denotes |
psychiatric |
DISEASE |
|
| T12871 |
390-394 |
GeneOrGeneProduct |
denotes |
WFS1 |
|
|
| T3 |
406-427 |
GeneOrGeneProduct |
denotes |
transmembrane protein |
|
|
| T11 |
471-474 |
DiseaseOrPhenotypicFeature |
denotes |
WFS |
D014929 |
|
| T4 |
559-563 |
GeneOrGeneProduct |
denotes |
WFS1 |
|
|
| T92757 |
578-586 |
OrganismTaxon |
denotes |
patients |
|
|
| T49754 |
691-699 |
OrganismTaxon |
denotes |
patients |
|
|
| T12 |
716-731 |
DiseaseOrPhenotypicFeature |
denotes |
hypopituitarism |
D007018 |
|
| T13 |
764-767 |
DiseaseOrPhenotypicFeature |
denotes |
WFS |
D014929 |
|
| T14 |
835-838 |
DiseaseOrPhenotypicFeature |
denotes |
WFS |
D014929 |
|
| T15 |
905-908 |
DiseaseOrPhenotypicFeature |
denotes |
WFS |
D014929 |
|
