| Id |
Subject |
Object |
Predicate |
Lexical cue |
| T1 |
6-10 |
GeneOrGeneProduct |
denotes |
base |
| T2 |
11-15 |
GeneOrGeneProduct |
denotes |
pair |
| T3 |
32-37 |
GeneOrGeneProduct |
denotes |
PQBP1 |
| T4 |
62-76 |
GeneOrGeneProduct |
denotes |
microphthalmia |
| T5 |
116-124 |
GeneOrGeneProduct |
denotes |
X-linked |
| T6 |
180-189 |
GeneOrGeneProduct |
denotes |
syndromic |
| T7 |
193-197 |
GeneOrGeneProduct |
denotes |
XLMR |
| T8 |
207-216 |
GeneOrGeneProduct |
denotes |
syndromic |
| T9 |
227-231 |
GeneOrGeneProduct |
denotes |
XLMR |
| T10 |
284-289 |
GeneOrGeneProduct |
denotes |
begin |
| T11 |
304-313 |
GeneOrGeneProduct |
denotes |
mutations |
| T12 |
344-349 |
GeneOrGeneProduct |
denotes |
PQBP1 |
| T13 |
363-367 |
GeneOrGeneProduct |
denotes |
XLMR |
| T14 |
382-386 |
GeneOrGeneProduct |
denotes |
XLMR |
| T15 |
444-452 |
GeneOrGeneProduct |
denotes |
X-linked |
| T16 |
491-505 |
GeneOrGeneProduct |
denotes |
microphthalmia |
| T17 |
561-568 |
GeneOrGeneProduct |
denotes |
spastic |
| T18 |
625-633 |
GeneOrGeneProduct |
denotes |
spanning |
| T19 |
638-644 |
GeneOrGeneProduct |
denotes |
entire |
| T20 |
645-657 |
GeneOrGeneProduct |
denotes |
X-chromosome |
| T21 |
694-696 |
GeneOrGeneProduct |
denotes |
Mb |
| T22 |
745-749 |
GeneOrGeneProduct |
denotes |
BCOR |
| T23 |
758-766 |
GeneOrGeneProduct |
denotes |
missense |
| T24 |
767-775 |
GeneOrGeneProduct |
denotes |
mutation |
| T25 |
779-783 |
GeneOrGeneProduct |
denotes |
BCOR |
| T26 |
798-802 |
GeneOrGeneProduct |
denotes |
in a |
| T27 |
820-834 |
GeneOrGeneProduct |
denotes |
microphthalmia |
| T28 |
835-843 |
GeneOrGeneProduct |
denotes |
syndrome |
| T29 |
947-958 |
GeneOrGeneProduct |
denotes |
no mutation |
| T30 |
966-970 |
GeneOrGeneProduct |
denotes |
BCOR |
| T31 |
1015-1023 |
GeneOrGeneProduct |
denotes |
mutation |
| T32 |
1036-1041 |
GeneOrGeneProduct |
denotes |
PQBP1 |
| T33 |
1111-1117 |
GeneOrGeneProduct |
denotes |
a 2-bp |
| T34 |
1198-1206 |
GeneOrGeneProduct |
denotes |
mutation |
| T35 |
1257-1265 |
GeneOrGeneProduct |
denotes |
syndrome |
| T36 |
1285-1289 |
GeneOrGeneProduct |
denotes |
XLMR |
| T37 |
1330-1339 |
GeneOrGeneProduct |
denotes |
mosaicism |
| T38 |
1435-1443 |
GeneOrGeneProduct |
denotes |
findings |
| T39 |
1470-1474 |
GeneOrGeneProduct |
denotes |
time |
| T40 |
1475-1489 |
GeneOrGeneProduct |
denotes |
that mutations |
| T41 |
1493-1498 |
GeneOrGeneProduct |
denotes |
PQBP1 |
| T42 |
1524-1528 |
GeneOrGeneProduct |
denotes |
XLMR |
| T43 |
1549-1563 |
GeneOrGeneProduct |
denotes |
microphthalmia |
| T44 |
1581-1590 |
GeneOrGeneProduct |
denotes |
extending |
| T45 |
1643-1648 |
GeneOrGeneProduct |
denotes |
PQBP1 |
| T46 |
1649-1658 |
GeneOrGeneProduct |
denotes |
mutations |
