| Id |
Subject |
Object |
Predicate |
Lexical cue |
db_id |
| 3995 |
16-29 |
GeneOrGeneProduct |
denotes |
synaptotagmin |
NCBIGene:255928 |
| 3996 |
31-36 |
GeneOrGeneProduct |
denotes |
SYT14 |
NCBIGene:255928 |
| 3997 |
54-86 |
DiseaseOrPhenotypicFeature |
denotes |
neurodevelopmental abnormalities |
MESH:D009421 |
| 3998 |
247-263 |
DiseaseOrPhenotypicFeature |
denotes |
cerebral atrophy |
MESH:D001927 |
| 3999 |
265-277 |
DiseaseOrPhenotypicFeature |
denotes |
macrocephaly |
MESH:D058627 |
| 4000 |
278-286 |
DiseaseOrPhenotypicFeature |
denotes |
seizures |
MESH:D012640 |
| 4001 |
292-311 |
DiseaseOrPhenotypicFeature |
denotes |
developmental delay |
MESH:D002658 |
| 4002 |
428-441 |
GeneOrGeneProduct |
denotes |
synaptotagmin |
NCBIGene:255928 |
| 4003 |
448-453 |
GeneOrGeneProduct |
denotes |
SYT14 |
NCBIGene:255928 |
| 4004 |
493-498 |
GeneOrGeneProduct |
denotes |
SYT14 |
NCBIGene:255928 |
| 4005 |
502-507 |
OrganismTaxon |
denotes |
human |
NCBITaxon:9606 |
| 4006 |
576-589 |
GeneOrGeneProduct |
denotes |
synaptotagmin |
NCBIGene:255928 |
| 4007 |
650-657 |
ChemicalEntity |
denotes |
calcium |
MESH:D002118 |
| 4008 |
761-766 |
GeneOrGeneProduct |
denotes |
SYT14 |
NCBIGene:255928 |
| 4009 |
899-904 |
GeneOrGeneProduct |
denotes |
SYT14 |
NCBIGene:255928 |
| 4010 |
1021-1026 |
GeneOrGeneProduct |
denotes |
SYT14 |
NCBIGene:255928 |
