| Id |
Subject |
Object |
Predicate |
Lexical cue |
| T1 |
28-46 |
DiseaseOrPhenotypicFeature |
denotes |
X linked nystagmus |
| T2 |
77-84 |
SequenceVariant |
denotes |
p.R229G |
| T3 |
111-116 |
GeneOrGeneProduct |
denotes |
FRMD7 |
| T4 |
173-187 |
DiseaseOrPhenotypicFeature |
denotes |
genetic defect |
| T5 |
207-225 |
DiseaseOrPhenotypicFeature |
denotes |
X linked nystagmus |
| T6 |
227-230 |
DiseaseOrPhenotypicFeature |
denotes |
NYS |
| T7 |
352-357 |
GeneOrGeneProduct |
denotes |
FRMD7 |
| T8 |
553-563 |
SequenceVariant |
denotes |
CAG repeat |
| T9 |
571-588 |
GeneOrGeneProduct |
denotes |
androgen receptor |
| T10 |
660-663 |
DiseaseOrPhenotypicFeature |
denotes |
NYS |
| T11 |
725-733 |
SequenceVariant |
denotes |
c.686C>G |
| T12 |
789-835 |
SequenceVariant |
denotes |
arginine at amino acid position 229 by glycine |
| T13 |
837-844 |
SequenceVariant |
denotes |
p.R229G |
| T14 |
863-868 |
GeneOrGeneProduct |
denotes |
FRMD7 |
| T15 |
1179-1186 |
SequenceVariant |
denotes |
p.R229G |
| T16 |
1203-1208 |
GeneOrGeneProduct |
denotes |
FRMD7 |
| T17 |
1225-1228 |
DiseaseOrPhenotypicFeature |
denotes |
NYS |
| T18 |
1313-1325 |
DiseaseOrPhenotypicFeature |
denotes |
X linked NYS |
