| Id |
Subject |
Object |
Predicate |
Lexical cue |
db_id |
| 6493 |
6-13 |
GeneOrGeneProduct |
denotes |
CACNA1S |
NCBIGene:779 |
| 6494 |
49-79 |
DiseaseOrPhenotypicFeature |
denotes |
hypokalemic periodic paralysis |
MESH:D020514 |
| 6495 |
108-139 |
DiseaseOrPhenotypicFeature |
denotes |
Hypokalaemic periodic paralysis |
MESH:D020514 |
| 6496 |
141-147 |
DiseaseOrPhenotypicFeature |
denotes |
HypoPP |
MESH:D020514 |
| 6497 |
155-182 |
DiseaseOrPhenotypicFeature |
denotes |
autosomal dominant disorder |
MESH:D030342 |
| 6498 |
230-245 |
DiseaseOrPhenotypicFeature |
denotes |
muscle weakness |
MESH:D018908 |
| 6499 |
286-295 |
ChemicalEntity |
denotes |
potassium |
MESH:D011188 |
| 6500 |
336-342 |
DiseaseOrPhenotypicFeature |
denotes |
HypoPP |
MESH:D020514 |
| 6501 |
366-373 |
GeneOrGeneProduct |
denotes |
CACNA1S |
NCBIGene:779 |
| 6502 |
393-438 |
GeneOrGeneProduct |
denotes |
skeletal muscle calcium channel alpha-subunit |
NCBIGene:779 |
| 6503 |
538-545 |
GeneOrGeneProduct |
denotes |
CACNA1S |
NCBIGene:779 |
| 6504 |
570-576 |
DiseaseOrPhenotypicFeature |
denotes |
HypoPP |
MESH:D020514 |
| 6505 |
577-585 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 6506 |
668-675 |
GeneOrGeneProduct |
denotes |
CACNA1S |
NCBIGene:779 |
| 6507 |
809-815 |
DiseaseOrPhenotypicFeature |
denotes |
HypoPP |
MESH:D020514 |
| 6508 |
853-858 |
SequenceVariant |
denotes |
V876E |
DBSNP:rs267606698 |
| 6509 |
875-881 |
DiseaseOrPhenotypicFeature |
denotes |
HypoPP |
MESH:D020514 |
| 6510 |
882-890 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 6511 |
1004-1009 |
SequenceVariant |
denotes |
V876E |
DBSNP:rs267606698 |
| 6512 |
1146-1151 |
DiseaseOrPhenotypicFeature |
denotes |
death |
MESH:D003643 |
| 6513 |
1194-1201 |
GeneOrGeneProduct |
denotes |
CACNA1S |
NCBIGene:779 |
| 6514 |
1229-1236 |
GeneOrGeneProduct |
denotes |
CACNA1S |
NCBIGene:779 |
| 6515 |
1263-1269 |
DiseaseOrPhenotypicFeature |
denotes |
HypoPP |
MESH:D020514 |
