| Id |
Subject |
Object |
Predicate |
Lexical cue |
db_id |
| 12662 |
47-58 |
GeneOrGeneProduct |
denotes |
hippocalcin |
NCBIGene:3208 |
| 12663 |
83-88 |
OrganismTaxon |
denotes |
human |
NCBITaxon:9606 |
| 12664 |
89-97 |
DiseaseOrPhenotypicFeature |
denotes |
dystonia |
MESH:D004421 |
| 12665 |
99-107 |
DiseaseOrPhenotypicFeature |
denotes |
Dystonia |
MESH:D004421 |
| 12666 |
113-143 |
DiseaseOrPhenotypicFeature |
denotes |
neurological movement disorder |
MESH:D009069 |
| 12667 |
326-330 |
SequenceVariant |
denotes |
T71N |
DBSNP:rs775863165 |
| 12668 |
335-340 |
SequenceVariant |
denotes |
A190T |
DBSNP:rs550921485 |
| 12669 |
348-371 |
GeneOrGeneProduct |
denotes |
neuronal calcium sensor |
NCBIGene:3208 |
| 12670 |
373-376 |
GeneOrGeneProduct |
denotes |
NCS |
NCBIGene:3208 |
| 12671 |
378-389 |
GeneOrGeneProduct |
denotes |
hippocalcin |
NCBIGene:3208 |
| 12672 |
430-455 |
DiseaseOrPhenotypicFeature |
denotes |
primary isolated dystonia |
MESH:D004421 |
| 12673 |
457-461 |
GeneOrGeneProduct |
denotes |
DYT2 |
NCBIGene:3208 |
| 12674 |
462-470 |
DiseaseOrPhenotypicFeature |
denotes |
dystonia |
MESH:D004421 |
| 12675 |
541-552 |
GeneOrGeneProduct |
denotes |
hippocalcin |
NCBIGene:3208 |
| 12676 |
639-650 |
GeneOrGeneProduct |
denotes |
hippocalcin |
NCBIGene:3208 |
| 12677 |
669-676 |
ChemicalEntity |
denotes |
calcium |
MESH:D002118 |
| 12678 |
707-737 |
GeneOrGeneProduct |
denotes |
voltage-gated calcium channels |
NCBIGene:783 |
| 12679 |
749-753 |
SequenceVariant |
denotes |
T71N |
DBSNP:rs775863165 |
| 12680 |
758-763 |
SequenceVariant |
denotes |
A190T |
DBSNP:rs550921485 |
| 12681 |
767-778 |
GeneOrGeneProduct |
denotes |
hippocalcin |
NCBIGene:3208 |
| 12682 |
805-812 |
ChemicalEntity |
denotes |
calcium |
MESH:D002118 |
| 12683 |
870-874 |
ChemicalEntity |
denotes |
Ca2+ |
MESH:D000069285 |
| 12684 |
937-948 |
GeneOrGeneProduct |
denotes |
hippocalcin |
NCBIGene:3208 |
| 12685 |
974-977 |
GeneOrGeneProduct |
denotes |
NCS |
NCBIGene:3208 |
| 12686 |
1324-1331 |
ChemicalEntity |
denotes |
calcium |
MESH:D002118 |
| 12687 |
1342-1345 |
ChemicalEntity |
denotes |
KCl |
MESH:D011189 |
| 12688 |
1383-1394 |
GeneOrGeneProduct |
denotes |
hippocalcin |
NCBIGene:3208 |
| 12689 |
1413-1450 |
GeneOrGeneProduct |
denotes |
N-type voltage-gated calcium channels |
NCBIGene:774 |
| 12690 |
1482-1490 |
DiseaseOrPhenotypicFeature |
denotes |
dystonia |
MESH:D004421 |
| 12691 |
1525-1536 |
GeneOrGeneProduct |
denotes |
hippocalcin |
NCBIGene:3208 |
| 12692 |
1599-1606 |
ChemicalEntity |
denotes |
calcium |
MESH:D002118 |
| 12693 |
1621-1625 |
GeneOrGeneProduct |
denotes |
DYT2 |
NCBIGene:3208 |
| 12694 |
1626-1634 |
DiseaseOrPhenotypicFeature |
denotes |
dystonia |
MESH:D004421 |
