| Id |
Subject |
Object |
Predicate |
Lexical cue |
db_id |
| 8325 |
6-12 |
GeneOrGeneProduct |
denotes |
CRELD1 |
NCBIGene:78987 |
| 8326 |
31-39 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 8327 |
45-75 |
DiseaseOrPhenotypicFeature |
denotes |
atrioventricular septal defect |
MESH:C562831 |
| 8328 |
89-120 |
DiseaseOrPhenotypicFeature |
denotes |
Atrioventricular septal defects |
MESH:C562831 |
| 8329 |
122-127 |
DiseaseOrPhenotypicFeature |
denotes |
AVSDs |
MESH:C562831 |
| 8330 |
190-216 |
DiseaseOrPhenotypicFeature |
denotes |
autosomal dominant defects |
MESH:D030342 |
| 8331 |
248-261 |
DiseaseOrPhenotypicFeature |
denotes |
malformations |
MESH:D000013 |
| 8332 |
394-398 |
DiseaseOrPhenotypicFeature |
denotes |
AVSD |
MESH:C562831 |
| 8333 |
400-406 |
GeneOrGeneProduct |
denotes |
CRELD1 |
NCBIGene:78987 |
| 8334 |
469-473 |
DiseaseOrPhenotypicFeature |
denotes |
AVSD |
MESH:C562831 |
| 8335 |
508-516 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 8336 |
522-526 |
DiseaseOrPhenotypicFeature |
denotes |
AVSD |
MESH:C562831 |
| 8337 |
644-650 |
GeneOrGeneProduct |
denotes |
CRELD1 |
NCBIGene:78987 |
| 8338 |
779-787 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 8339 |
816-823 |
OrganismTaxon |
denotes |
patient |
NCBITaxon:9606 |
| 8340 |
827-877 |
SequenceVariant |
denotes |
C-to-G transition was identified at nucleotide 857 |
c|SUB|C|857|G |
| 8341 |
923-960 |
SequenceVariant |
denotes |
alanine for proline at amino acid 286 |
p|SUB|A|286|P |
| 8342 |
974-981 |
ChemicalEntity |
denotes |
calcium |
MESH:D002118 |
| 8343 |
990-993 |
GeneOrGeneProduct |
denotes |
EGF |
NCBIGene:1950 |
| 8344 |
1007-1014 |
OrganismTaxon |
denotes |
patient |
NCBITaxon:9606 |
| 8345 |
1039-1043 |
DiseaseOrPhenotypicFeature |
denotes |
AVSD |
MESH:C562831 |
| 8346 |
1127-1134 |
OrganismTaxon |
denotes |
patient |
NCBITaxon:9606 |
| 8347 |
1150-1154 |
DiseaseOrPhenotypicFeature |
denotes |
AVSD |
MESH:C562831 |
| 8348 |
1171-1184 |
DiseaseOrPhenotypicFeature |
denotes |
Down syndrome |
MESH:D004314 |
| 8349 |
1203-1211 |
SequenceVariant |
denotes |
c.973G>A |
DBSNP:rs755981922 |
| 8350 |
1263-1305 |
SequenceVariant |
denotes |
lysine for glutamic acid at amino acid 325 |
DBSNP:rs755981922 |
| 8351 |
1307-1312 |
SequenceVariant |
denotes |
E325K |
DBSNP:rs755981922 |
| 8352 |
1328-1335 |
ChemicalEntity |
denotes |
calcium |
MESH:D002118 |
| 8353 |
1344-1347 |
GeneOrGeneProduct |
denotes |
EGF |
NCBIGene:1950 |
| 8354 |
1379-1385 |
GeneOrGeneProduct |
denotes |
CRELD1 |
NCBIGene:78987 |
| 8355 |
1419-1426 |
ChemicalEntity |
denotes |
calcium |
MESH:D002118 |
| 8356 |
1435-1438 |
GeneOrGeneProduct |
denotes |
EGF |
NCBIGene:1950 |
| 8357 |
1449-1457 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 8358 |
1463-1467 |
DiseaseOrPhenotypicFeature |
denotes |
AVSD |
MESH:C562831 |
| 8359 |
1469-1475 |
GeneOrGeneProduct |
denotes |
CRELD1 |
NCBIGene:78987 |
| 8360 |
1495-1499 |
DiseaseOrPhenotypicFeature |
denotes |
AVSD |
MESH:C562831 |
| 8361 |
1524-1530 |
GeneOrGeneProduct |
denotes |
CRELD1 |
NCBIGene:78987 |
| 8362 |
1579-1591 |
DiseaseOrPhenotypicFeature |
denotes |
heart defect |
MESH:D006331 |
