| Id |
Subject |
Object |
Predicate |
Lexical cue |
db_id |
| 652 |
28-36 |
ChemicalEntity |
denotes |
thiazide |
MESH:D049971 |
| 653 |
47-67 |
GeneOrGeneProduct |
denotes |
Na-Cl co-transporter |
NCBIGene:6559 |
| 654 |
85-93 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 655 |
99-118 |
DiseaseOrPhenotypicFeature |
denotes |
Gitelman's syndrome |
MESH:D053579 |
| 656 |
132-151 |
DiseaseOrPhenotypicFeature |
denotes |
Gitelman's syndrome |
MESH:D053579 |
| 657 |
153-155 |
DiseaseOrPhenotypicFeature |
denotes |
GS |
MESH:D053579 |
| 658 |
163-191 |
DiseaseOrPhenotypicFeature |
denotes |
autosomal recessive disorder |
MESH:D030342 |
| 659 |
237-245 |
ChemicalEntity |
denotes |
thiazide |
MESH:D049971 |
| 660 |
256-276 |
GeneOrGeneProduct |
denotes |
Na-Cl co-transporter |
NCBIGene:6559 |
| 661 |
278-282 |
GeneOrGeneProduct |
denotes |
NCCT |
NCBIGene:6559 |
| 662 |
463-467 |
GeneOrGeneProduct |
denotes |
NCCT |
NCBIGene:6559 |
| 663 |
491-499 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 664 |
505-507 |
DiseaseOrPhenotypicFeature |
denotes |
GS |
MESH:D053579 |
| 665 |
572-580 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 666 |
586-588 |
DiseaseOrPhenotypicFeature |
denotes |
GS |
MESH:D053579 |
| 667 |
668-672 |
GeneOrGeneProduct |
denotes |
NCCT |
NCBIGene:6559 |
| 668 |
790-798 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 669 |
930-938 |
SequenceVariant |
denotes |
c.185C>T |
DBSNP:rs371443644 |
| 670 |
940-948 |
SequenceVariant |
denotes |
Thr60Met |
DBSNP:rs371443644 |
| 671 |
951-960 |
SequenceVariant |
denotes |
c.1712C>T |
DBSNP:rs79351185 |
| 672 |
962-971 |
SequenceVariant |
denotes |
Ala569Val |
DBSNP:rs79351185 |
| 673 |
974-983 |
SequenceVariant |
denotes |
c.1930C>T |
DBSNP:rs200697179 |
| 674 |
985-994 |
SequenceVariant |
denotes |
Arg642Cys |
DBSNP:rs200697179 |
| 675 |
997-1006 |
SequenceVariant |
denotes |
c.2552T>A |
DBSNP:rs185927948 |
| 676 |
1008-1017 |
SequenceVariant |
denotes |
Leu849His |
DBSNP:rs185927948 |
| 677 |
1023-1033 |
SequenceVariant |
denotes |
c.1932delC |
c|DEL|1932|C |
| 678 |
1066-1074 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 679 |
1087-1089 |
DiseaseOrPhenotypicFeature |
denotes |
GS |
MESH:D053579 |
| 680 |
1090-1098 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 681 |
1155-1161 |
SequenceVariant |
denotes |
c.7A>T |
c|SUB|A|7|T |
| 682 |
1163-1170 |
SequenceVariant |
denotes |
Met1Leu |
p|SUB|M|1|L |
| 683 |
1173-1192 |
SequenceVariant |
denotes |
c.1181_1186+20del26 |
c|DEL|1181_1186+20|26 |
| 684 |
1194-1210 |
SequenceVariant |
denotes |
c.1811_1812delAT |
c|DEL|1811_1812|AT |
| 685 |
1215-1225 |
SequenceVariant |
denotes |
IVS16+1G>A |
c|SUB|G|IVS16+1|A |
| 686 |
1262-1269 |
OrganismTaxon |
denotes |
patient |
NCBITaxon:9606 |
| 687 |
1275-1294 |
SequenceVariant |
denotes |
c.1181_1186+20del26 |
c|DEL|1181_1186+20|26 |
| 688 |
1394-1402 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 689 |
1408-1418 |
SequenceVariant |
denotes |
IVS16+1G>A |
c|SUB|G|IVS16+1|A |
| 690 |
1434-1449 |
SequenceVariant |
denotes |
96 bp insertion |
c|INS||96 |
| 691 |
1505-1513 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 692 |
1655-1659 |
GeneOrGeneProduct |
denotes |
NCCT |
NCBIGene:6559 |
| 693 |
1683-1691 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 694 |
1697-1699 |
DiseaseOrPhenotypicFeature |
denotes |
GS |
MESH:D053579 |
| 695 |
1772-1776 |
GeneOrGeneProduct |
denotes |
NCCT |
NCBIGene:6559 |
| 696 |
1794-1796 |
DiseaseOrPhenotypicFeature |
denotes |
GS |
MESH:D053579 |
| 697 |
1797-1805 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
