| Id |
Subject |
Object |
Predicate |
Lexical cue |
db_id |
| 3446 |
32-37 |
GeneOrGeneProduct |
denotes |
PQBP1 |
NCBIGene:10084 |
| 3447 |
62-76 |
DiseaseOrPhenotypicFeature |
denotes |
microphthalmia |
MESH:D008850 |
| 3448 |
78-90 |
DiseaseOrPhenotypicFeature |
denotes |
microcephaly |
MESH:D008831 |
| 3449 |
96-114 |
DiseaseOrPhenotypicFeature |
denotes |
mental retardation |
MESH:D008607 |
| 3450 |
116-143 |
DiseaseOrPhenotypicFeature |
denotes |
X-linked mental retardation |
MESH:D038901 |
| 3451 |
193-197 |
DiseaseOrPhenotypicFeature |
denotes |
XLMR |
MESH:D038901 |
| 3452 |
227-231 |
DiseaseOrPhenotypicFeature |
denotes |
XLMR |
MESH:D038901 |
| 3453 |
344-349 |
GeneOrGeneProduct |
denotes |
PQBP1 |
NCBIGene:10084 |
| 3454 |
363-367 |
DiseaseOrPhenotypicFeature |
denotes |
XLMR |
MESH:D038901 |
| 3455 |
382-386 |
DiseaseOrPhenotypicFeature |
denotes |
XLMR |
MESH:D038901 |
| 3456 |
444-484 |
DiseaseOrPhenotypicFeature |
denotes |
X-linked phenotype of mental retardation |
MESH:D038901 |
| 3457 |
486-488 |
DiseaseOrPhenotypicFeature |
denotes |
MR |
MESH:D008607 |
| 3458 |
491-505 |
DiseaseOrPhenotypicFeature |
denotes |
microphthalmia |
MESH:D008850 |
| 3459 |
507-523 |
DiseaseOrPhenotypicFeature |
denotes |
choroid coloboma |
MESH:D003103 |
| 3460 |
525-537 |
DiseaseOrPhenotypicFeature |
denotes |
microcephaly |
MESH:D008831 |
| 3461 |
539-555 |
DiseaseOrPhenotypicFeature |
denotes |
renal hypoplasia |
MESH:D007674 |
| 3462 |
561-579 |
DiseaseOrPhenotypicFeature |
denotes |
spastic paraplegia |
MESH:D010264 |
| 3463 |
745-749 |
GeneOrGeneProduct |
denotes |
BCOR |
NCBIGene:54880 |
| 3464 |
779-783 |
GeneOrGeneProduct |
denotes |
BCOR |
NCBIGene:54880 |
| 3465 |
815-843 |
DiseaseOrPhenotypicFeature |
denotes |
Lenz microphthalmia syndrome |
MESH:C537464 |
| 3466 |
966-970 |
GeneOrGeneProduct |
denotes |
BCOR |
NCBIGene:54880 |
| 3467 |
994-1002 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 3468 |
1036-1041 |
GeneOrGeneProduct |
denotes |
PQBP1 |
NCBIGene:10084 |
| 3469 |
1128-1142 |
SequenceVariant |
denotes |
c.461_462delAG |
DBSNP:rs606231195 |
| 3470 |
1230-1265 |
DiseaseOrPhenotypicFeature |
denotes |
Hamel cerebropalatocardiac syndrome |
MESH:C537761 |
| 3471 |
1285-1289 |
DiseaseOrPhenotypicFeature |
denotes |
XLMR |
MESH:D038901 |
| 3472 |
1493-1498 |
GeneOrGeneProduct |
denotes |
PQBP1 |
NCBIGene:10084 |
| 3473 |
1524-1528 |
DiseaseOrPhenotypicFeature |
denotes |
XLMR |
MESH:D038901 |
| 3474 |
1549-1563 |
DiseaseOrPhenotypicFeature |
denotes |
microphthalmia |
MESH:D008850 |
| 3475 |
1643-1648 |
GeneOrGeneProduct |
denotes |
PQBP1 |
NCBIGene:10084 |
