| Id |
Subject |
Object |
Predicate |
Lexical cue |
| T1 |
28-36 |
ChemicalEntity |
denotes |
thiazide |
| T2 |
47-67 |
GeneOrGeneProduct |
denotes |
Na-Cl co-transporter |
| T3 |
85-93 |
OrganismTaxon |
denotes |
patients |
| T4 |
99-118 |
DiseaseOrPhenotypicFeature |
denotes |
Gitelman's syndrome |
| T5 |
132-151 |
DiseaseOrPhenotypicFeature |
denotes |
Gitelman's syndrome |
| T6 |
153-155 |
DiseaseOrPhenotypicFeature |
denotes |
GS |
| T7 |
163-191 |
DiseaseOrPhenotypicFeature |
denotes |
autosomal recessive disorder |
| T8 |
237-245 |
ChemicalEntity |
denotes |
thiazide |
| T9 |
256-276 |
GeneOrGeneProduct |
denotes |
Na-Cl co-transporter |
| T10 |
278-282 |
GeneOrGeneProduct |
denotes |
NCCT |
| T11 |
463-467 |
GeneOrGeneProduct |
denotes |
NCCT |
| T12 |
491-499 |
OrganismTaxon |
denotes |
patients |
| T13 |
505-507 |
DiseaseOrPhenotypicFeature |
denotes |
GS |
| T14 |
572-580 |
OrganismTaxon |
denotes |
patients |
| T15 |
586-588 |
DiseaseOrPhenotypicFeature |
denotes |
GS |
| T16 |
668-672 |
GeneOrGeneProduct |
denotes |
NCCT |
| T17 |
790-798 |
OrganismTaxon |
denotes |
patients |
| T18 |
930-938 |
SequenceVariant |
denotes |
c.185C>T |
| T19 |
940-948 |
SequenceVariant |
denotes |
Thr60Met |
| T20 |
951-960 |
SequenceVariant |
denotes |
c.1712C>T |
| T21 |
962-971 |
SequenceVariant |
denotes |
Ala569Val |
| T22 |
974-983 |
SequenceVariant |
denotes |
c.1930C>T |
| T23 |
985-994 |
SequenceVariant |
denotes |
Arg642Cys |
| T24 |
997-1006 |
SequenceVariant |
denotes |
c.2552T>A |
| T25 |
1008-1017 |
SequenceVariant |
denotes |
Leu849His |
| T26 |
1023-1033 |
SequenceVariant |
denotes |
c.1932delC |
| T27 |
1066-1074 |
OrganismTaxon |
denotes |
patients |
| T28 |
1087-1089 |
DiseaseOrPhenotypicFeature |
denotes |
GS |
| T29 |
1090-1098 |
OrganismTaxon |
denotes |
patients |
| T30 |
1155-1161 |
SequenceVariant |
denotes |
c.7A>T |
| T31 |
1163-1170 |
SequenceVariant |
denotes |
Met1Leu |
| T32 |
1173-1192 |
SequenceVariant |
denotes |
c.1181_1186+20del26 |
| T33 |
1194-1210 |
SequenceVariant |
denotes |
c.1811_1812delAT |
| T34 |
1215-1225 |
SequenceVariant |
denotes |
IVS16+1G>A |
| T35 |
1262-1269 |
OrganismTaxon |
denotes |
patient |
| T36 |
1275-1294 |
SequenceVariant |
denotes |
c.1181_1186+20del26 |
| T37 |
1394-1402 |
OrganismTaxon |
denotes |
patients |
| T38 |
1408-1418 |
SequenceVariant |
denotes |
IVS16+1G>A |
| T39 |
1434-1449 |
SequenceVariant |
denotes |
96 bp insertion |
| T40 |
1505-1513 |
OrganismTaxon |
denotes |
patients |
| T41 |
1655-1659 |
GeneOrGeneProduct |
denotes |
NCCT |
| T42 |
1683-1691 |
OrganismTaxon |
denotes |
patients |
| T43 |
1697-1699 |
DiseaseOrPhenotypicFeature |
denotes |
GS |
| T44 |
1772-1776 |
GeneOrGeneProduct |
denotes |
NCCT |
| T45 |
1794-1796 |
DiseaseOrPhenotypicFeature |
denotes |
GS |
| T46 |
1797-1805 |
OrganismTaxon |
denotes |
patients |
