| Id |
Subject |
Object |
Predicate |
Lexical cue |
#label |
ID: |
| T26469 |
77-84 |
SequenceVariant |
denotes |
p.R229G |
|
|
| T5223 |
111-116 |
GeneOrGeneProduct |
denotes |
FRMD7 |
|
|
| T1 |
173-187 |
DiseaseOrPhenotypicFeature |
denotes |
genetic defect |
DISEASE |
|
| T2 |
254-258 |
GeneOrGeneProduct |
denotes |
Xp11 |
|
|
| T3 |
352-357 |
GeneOrGeneProduct |
denotes |
FRMD7 |
|
|
| T4 |
399-411 |
GeneOrGeneProduct |
denotes |
X chromosome |
|
|
| T5 |
571-588 |
GeneOrGeneProduct |
denotes |
androgen receptor |
|
|
| T61695 |
725-733 |
SequenceVariant |
denotes |
c.686C>G |
|
|
| T47011 |
789-797 |
ChemicalEntity |
denotes |
arginine |
|
http://purl.obolibrary.org/obo/CHEBI_16467|http://purl.obolibrary.org/obo/CHEBI_29016|http://purl.obolibrary.org/obo/CHEBI_32696 |
| T22164 |
828-835 |
ChemicalEntity |
denotes |
glycine |
|
http://purl.obolibrary.org/obo/CHEBI_15428|http://purl.obolibrary.org/obo/CHEBI_29947|http://purl.obolibrary.org/obo/CHEBI_57305 |
| T86947 |
837-844 |
SequenceVariant |
denotes |
p.R229G |
|
|
| T6 |
863-868 |
GeneOrGeneProduct |
denotes |
FRMD7 |
|
|
| T5327 |
1179-1186 |
SequenceVariant |
denotes |
p.R229G |
|
|
| T7 |
1203-1208 |
GeneOrGeneProduct |
denotes |
FRMD7 |
|
|
