| Id |
Subject |
Object |
Predicate |
Lexical cue |
#label |
| T1 |
32-37 |
GeneOrGeneProduct |
denotes |
PQBP1 |
|
| T21811 |
62-76 |
DiseaseOrPhenotypicFeature |
denotes |
microphthalmia |
D008850 |
| T61537 |
78-90 |
DiseaseOrPhenotypicFeature |
denotes |
microcephaly |
D008831 |
| T12538 |
96-114 |
DiseaseOrPhenotypicFeature |
denotes |
mental retardation |
D008607 |
| T30956 |
116-143 |
DiseaseOrPhenotypicFeature |
denotes |
X-linked mental retardation |
D038901 |
| T59750 |
193-197 |
DiseaseOrPhenotypicFeature |
denotes |
XLMR |
DISEASE |
| T6556 |
227-231 |
DiseaseOrPhenotypicFeature |
denotes |
XLMR |
DISEASE |
| T2 |
344-349 |
GeneOrGeneProduct |
denotes |
PQBP1 |
|
| T87219 |
363-367 |
DiseaseOrPhenotypicFeature |
denotes |
XLMR |
DISEASE |
| T44580 |
382-386 |
DiseaseOrPhenotypicFeature |
denotes |
XLMR |
DISEASE |
| T96765 |
444-484 |
DiseaseOrPhenotypicFeature |
denotes |
X-linked phenotype of mental retardation |
DISEASE |
| T10 |
486-488 |
DiseaseOrPhenotypicFeature |
denotes |
MR |
D008607 |
| T11 |
491-505 |
DiseaseOrPhenotypicFeature |
denotes |
microphthalmia |
D008850 |
| T12 |
515-523 |
DiseaseOrPhenotypicFeature |
denotes |
coloboma |
D003103 |
| T13 |
525-537 |
DiseaseOrPhenotypicFeature |
denotes |
microcephaly |
D008831 |
| T14 |
539-555 |
DiseaseOrPhenotypicFeature |
denotes |
renal hypoplasia |
DISEASE |
| T15 |
561-579 |
DiseaseOrPhenotypicFeature |
denotes |
spastic paraplegia |
D010264 |
| T3 |
645-657 |
GeneOrGeneProduct |
denotes |
X-chromosome |
|
| T4 |
745-749 |
GeneOrGeneProduct |
denotes |
BCOR |
|
| T5 |
779-783 |
GeneOrGeneProduct |
denotes |
BCOR |
|
| T16 |
815-843 |
DiseaseOrPhenotypicFeature |
denotes |
Lenz microphthalmia syndrome |
C537464 |
| T6 |
966-970 |
GeneOrGeneProduct |
denotes |
BCOR |
|
| T38739 |
994-1002 |
OrganismTaxon |
denotes |
patients |
|
| T7 |
1036-1041 |
GeneOrGeneProduct |
denotes |
PQBP1 |
|
| T19725 |
1113-1126 |
SequenceVariant |
denotes |
2-bp deletion |
|
| T37958 |
1128-1142 |
SequenceVariant |
denotes |
c.461_462delAG |
|
| T17 |
1230-1265 |
DiseaseOrPhenotypicFeature |
denotes |
Hamel cerebropalatocardiac syndrome |
C537761 |
| T18 |
1285-1289 |
DiseaseOrPhenotypicFeature |
denotes |
XLMR |
DISEASE |
| T38142 |
1347-1360 |
SequenceVariant |
denotes |
2-bp deletion |
|
| T8 |
1493-1498 |
GeneOrGeneProduct |
denotes |
PQBP1 |
|
| T19 |
1524-1528 |
DiseaseOrPhenotypicFeature |
denotes |
XLMR |
DISEASE |
| T20 |
1549-1563 |
DiseaseOrPhenotypicFeature |
denotes |
microphthalmia |
D008850 |
| T9 |
1643-1648 |
GeneOrGeneProduct |
denotes |
PQBP1 |
|
