| Id |
Subject |
Object |
Predicate |
Lexical cue |
db_id |
| 5344 |
0-5 |
GeneOrGeneProduct |
denotes |
GATA4 |
NCBIGene:2626 |
| 5345 |
31-39 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 5346 |
45-69 |
DiseaseOrPhenotypicFeature |
denotes |
congenital heart disease |
MESH:D006331 |
| 5347 |
122-127 |
GeneOrGeneProduct |
denotes |
GATA4 |
NCBIGene:2626 |
| 5348 |
150-174 |
DiseaseOrPhenotypicFeature |
denotes |
congenital heart disease |
MESH:D006331 |
| 5349 |
176-179 |
DiseaseOrPhenotypicFeature |
denotes |
CHD |
MESH:D006331 |
| 5350 |
209-214 |
GeneOrGeneProduct |
denotes |
GATA4 |
NCBIGene:2626 |
| 5351 |
228-231 |
DiseaseOrPhenotypicFeature |
denotes |
CHD |
MESH:D006331 |
| 5352 |
264-269 |
GeneOrGeneProduct |
denotes |
GATA4 |
NCBIGene:2626 |
| 5353 |
283-286 |
DiseaseOrPhenotypicFeature |
denotes |
CHD |
MESH:D006331 |
| 5354 |
424-429 |
GeneOrGeneProduct |
denotes |
GATA4 |
NCBIGene:2626 |
| 5355 |
442-445 |
DiseaseOrPhenotypicFeature |
denotes |
CHD |
MESH:D006331 |
| 5356 |
446-454 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 5357 |
623-629 |
SequenceVariant |
denotes |
46delS |
|DEL|46|S |
| 5358 |
663-674 |
SequenceVariant |
denotes |
118-119insA |
|INS|118_119|A |
| 5359 |
679-691 |
SequenceVariant |
denotes |
125-126insAA |
|INS|125_126|AA |
| 5360 |
728-731 |
SequenceVariant |
denotes |
A6V |
DBSNP:rs199922907 |
| 5361 |
733-738 |
SequenceVariant |
denotes |
P163S |
DBSNP:rs387906769 |
| 5362 |
740-745 |
SequenceVariant |
denotes |
E359K |
DBSNP:rs368489876 |
| 5363 |
747-752 |
SequenceVariant |
denotes |
P407Q |
DBSNP:rs115099192 |
| 5364 |
754-759 |
SequenceVariant |
denotes |
S429T |
p|SUB|S|429|T |
| 5365 |
764-769 |
SequenceVariant |
denotes |
A442V |
DBSNP:rs146017816 |
| 5366 |
804-812 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 5367 |
824-849 |
DiseaseOrPhenotypicFeature |
denotes |
ventricular septal defect |
MESH:D006345 |
| 5368 |
860-879 |
DiseaseOrPhenotypicFeature |
denotes |
Tetralogy of Fallot |
MESH:D013771 |
| 5369 |
894-920 |
DiseaseOrPhenotypicFeature |
denotes |
endocardial cushion defect |
MESH:D004694 |
| 5370 |
936-944 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 5371 |
954-959 |
SequenceVariant |
denotes |
E359K |
DBSNP:rs368489876 |
| 5372 |
1014-1039 |
DiseaseOrPhenotypicFeature |
denotes |
ventricular septal defect |
MESH:D006345 |
| 5373 |
1041-1044 |
DiseaseOrPhenotypicFeature |
denotes |
VSD |
MESH:D006345 |
| 5374 |
1088-1101 |
SequenceVariant |
denotes |
c.1146+25insA |
c|INS|1146+25|A |
| 5375 |
1133-1136 |
DiseaseOrPhenotypicFeature |
denotes |
VSD |
MESH:D006345 |
| 5376 |
1137-1145 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 5377 |
1246-1251 |
GeneOrGeneProduct |
denotes |
GATA4 |
NCBIGene:2626 |
| 5378 |
1294-1299 |
GeneOrGeneProduct |
denotes |
GATA4 |
NCBIGene:2626 |
| 5379 |
1317-1320 |
DiseaseOrPhenotypicFeature |
denotes |
CHD |
MESH:D006331 |
| 5380 |
1342-1350 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
