| Id |
Subject |
Object |
Predicate |
Lexical cue |
| T1 |
63-67 |
GeneOrGeneProduct |
denotes |
SOX2 |
| T2 |
72-77 |
GeneOrGeneProduct |
denotes |
CHX10 |
| T3 |
87-95 |
OrganismTaxon |
denotes |
patients |
| T4 |
101-113 |
DiseaseOrPhenotypicFeature |
denotes |
anophthalmia |
| T5 |
114-128 |
DiseaseOrPhenotypicFeature |
denotes |
microphthalmia |
| T6 |
156-160 |
GeneOrGeneProduct |
denotes |
SOX2 |
| T7 |
165-170 |
GeneOrGeneProduct |
denotes |
CHX10 |
| T8 |
199-207 |
OrganismTaxon |
denotes |
patients |
| T9 |
213-225 |
DiseaseOrPhenotypicFeature |
denotes |
anophthalmia |
| T10 |
233-247 |
DiseaseOrPhenotypicFeature |
denotes |
microphthalmia |
| T11 |
280-292 |
DiseaseOrPhenotypicFeature |
denotes |
anophthalmic |
| T12 |
293-307 |
DiseaseOrPhenotypicFeature |
denotes |
microphthalmic |
| T13 |
308-315 |
OrganismTaxon |
denotes |
patient |
| T14 |
399-403 |
GeneOrGeneProduct |
denotes |
SOX2 |
| T15 |
408-413 |
GeneOrGeneProduct |
denotes |
CHX10 |
| T16 |
501-505 |
GeneOrGeneProduct |
denotes |
SOX2 |
| T17 |
510-515 |
GeneOrGeneProduct |
denotes |
CHX10 |
| T18 |
634-641 |
OrganismTaxon |
denotes |
Patient |
| T19 |
734-738 |
GeneOrGeneProduct |
denotes |
SOX2 |
| T20 |
743-748 |
GeneOrGeneProduct |
denotes |
CHX10 |
| T21 |
797-804 |
OrganismTaxon |
denotes |
patient |
| T22 |
897-901 |
GeneOrGeneProduct |
denotes |
SOX2 |
| T23 |
943-952 |
SequenceVariant |
denotes |
c.310 G>T |
| T24 |
954-964 |
SequenceVariant |
denotes |
p. Glu104X |
| T25 |
980-987 |
OrganismTaxon |
denotes |
patient |
| T26 |
1095-1124 |
SequenceVariant |
denotes |
glutamic acid to a stop codon |
| T27 |
1212-1221 |
SequenceVariant |
denotes |
c.549delC |
| T28 |
1223-1240 |
SequenceVariant |
denotes |
p. Pro184ArgfsX19 |
| T29 |
1476-1485 |
SequenceVariant |
denotes |
c.*557G>A |
| T30 |
1538-1545 |
OrganismTaxon |
denotes |
patient |
| T31 |
1677-1688 |
SequenceVariant |
denotes |
c. *469 C>A |
| T32 |
1694-1704 |
SequenceVariant |
denotes |
rs11915160 |
| T33 |
1739-1747 |
OrganismTaxon |
denotes |
patients |
| T34 |
1762-1767 |
GeneOrGeneProduct |
denotes |
CHX10 |
| T35 |
1813-1822 |
SequenceVariant |
denotes |
c.471 C>T |
| T36 |
1824-1835 |
SequenceVariant |
denotes |
p.Ser157Ser |
| T37 |
1837-1847 |
SequenceVariant |
denotes |
rs35435463 |
| T38 |
1853-1862 |
SequenceVariant |
denotes |
c.579 G>A |
| T39 |
1864-1876 |
SequenceVariant |
denotes |
p. Gln193Gln |
| T40 |
1931-1940 |
SequenceVariant |
denotes |
c.871 G>A |
| T41 |
1942-1954 |
SequenceVariant |
denotes |
p. Asp291Asn |
| T42 |
2111-2115 |
GeneOrGeneProduct |
denotes |
SOX2 |
| T43 |
2147-2151 |
GeneOrGeneProduct |
denotes |
SOX2 |
| T44 |
2179-2195 |
DiseaseOrPhenotypicFeature |
denotes |
eye malformation |
| T45 |
2197-2202 |
GeneOrGeneProduct |
denotes |
CHX10 |
| T46 |
2227-2241 |
DiseaseOrPhenotypicFeature |
denotes |
microphthalmia |
| T47 |
2242-2254 |
DiseaseOrPhenotypicFeature |
denotes |
anophthalmia |
| T48 |
2262-2269 |
OrganismTaxon |
denotes |
patient |
