| Id |
Subject |
Object |
Predicate |
Lexical cue |
| T1 |
13-17 |
GeneOrGeneProduct |
denotes |
POLG |
| T2 |
98-105 |
OrganismTaxon |
denotes |
patient |
| T3 |
111-126 |
DiseaseOrPhenotypicFeature |
denotes |
Alpers syndrome |
| T4 |
128-143 |
DiseaseOrPhenotypicFeature |
denotes |
Alpers syndrome |
| T5 |
170-197 |
DiseaseOrPhenotypicFeature |
denotes |
mitochondrial DNA depletion |
| T6 |
301-314 |
DiseaseOrPhenotypicFeature |
denotes |
liver disease |
| T7 |
368-372 |
GeneOrGeneProduct |
denotes |
POLG |
| T8 |
426-435 |
GeneOrGeneProduct |
denotes |
pol gamma |
| T9 |
443-451 |
OrganismTaxon |
denotes |
patients |
| T10 |
457-472 |
DiseaseOrPhenotypicFeature |
denotes |
Alpers syndrome |
| T11 |
569-573 |
GeneOrGeneProduct |
denotes |
POLG |
| T12 |
581-585 |
GeneOrGeneProduct |
denotes |
POLG |
| T13 |
758-765 |
OrganismTaxon |
denotes |
patient |
| T14 |
771-786 |
DiseaseOrPhenotypicFeature |
denotes |
Alpers syndrome |
| T15 |
807-815 |
SequenceVariant |
denotes |
E873stop |
| T16 |
816-821 |
SequenceVariant |
denotes |
A467T |
| T17 |
827-835 |
SequenceVariant |
denotes |
E873stop |
| T18 |
906-911 |
SequenceVariant |
denotes |
A467T |
| T19 |
932-952 |
SequenceVariant |
denotes |
threonine to alanine |
| T20 |
1039-1047 |
SequenceVariant |
denotes |
E873-TAG |
| T21 |
1147-1156 |
GeneOrGeneProduct |
denotes |
pol gamma |
| T22 |
1372-1376 |
GeneOrGeneProduct |
denotes |
POLG |
| T23 |
1422-1427 |
SequenceVariant |
denotes |
A467T |
| T24 |
1468-1476 |
SequenceVariant |
denotes |
E873stop |
| T25 |
1527-1531 |
GeneOrGeneProduct |
denotes |
POLG |
| T26 |
1575-1580 |
SequenceVariant |
denotes |
A467T |
| T27 |
1629-1636 |
OrganismTaxon |
denotes |
patient |
| T28 |
1689-1694 |
SequenceVariant |
denotes |
A467T |
| T29 |
1756-1764 |
SequenceVariant |
denotes |
E873stop |
