| Id |
Subject |
Object |
Predicate |
Lexical cue |
db_id |
| 6859 |
77-83 |
GeneOrGeneProduct |
denotes |
Klotho |
NCBIGene:9365 |
| 6860 |
112-134 |
DiseaseOrPhenotypicFeature |
denotes |
essential hypertension |
MESH:D000075222 |
| 6861 |
178-182 |
OrganismTaxon |
denotes |
Mice |
NCBITaxon:10090 |
| 6862 |
203-209 |
GeneOrGeneProduct |
denotes |
Klotho |
NCBIGene:16591 |
| 6863 |
259-275 |
DiseaseOrPhenotypicFeature |
denotes |
arteriosclerosis |
MESH:D001161 |
| 6864 |
302-308 |
SequenceVariant |
denotes |
G-395A |
DBSNP:rs1207568 |
| 6865 |
352-357 |
OrganismTaxon |
denotes |
human |
NCBITaxon:9606 |
| 6866 |
358-364 |
GeneOrGeneProduct |
denotes |
Klotho |
NCBIGene:9365 |
| 6867 |
406-428 |
DiseaseOrPhenotypicFeature |
denotes |
Essential Hypertension |
MESH:D000075222 |
| 6868 |
430-432 |
DiseaseOrPhenotypicFeature |
denotes |
EH |
MESH:D000075222 |
| 6869 |
471-477 |
SequenceVariant |
denotes |
G-395A |
DBSNP:rs1207568 |
| 6870 |
494-500 |
GeneOrGeneProduct |
denotes |
Klotho |
NCBIGene:9365 |
| 6871 |
520-522 |
DiseaseOrPhenotypicFeature |
denotes |
EH |
MESH:D000075222 |
| 6872 |
557-565 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 6873 |
571-573 |
DiseaseOrPhenotypicFeature |
denotes |
EH |
MESH:D000075222 |
| 6874 |
586-598 |
DiseaseOrPhenotypicFeature |
denotes |
hypertensive |
MESH:D006973 |
| 6875 |
634-637 |
SequenceVariant |
denotes |
G/A |
DBSNP:rs1207568 |
| 6876 |
658-664 |
SequenceVariant |
denotes |
G-395A |
DBSNP:rs1207568 |
| 6877 |
814-820 |
SequenceVariant |
denotes |
G-395A |
DBSNP:rs1207568 |
| 6878 |
846-848 |
DiseaseOrPhenotypicFeature |
denotes |
EH |
MESH:D000075222 |
| 6879 |
857-869 |
DiseaseOrPhenotypicFeature |
denotes |
hypertension |
MESH:D006973 |
| 6880 |
1009-1015 |
SequenceVariant |
denotes |
G-395A |
DBSNP:rs1207568 |
| 6881 |
1034-1036 |
DiseaseOrPhenotypicFeature |
denotes |
EH |
MESH:D000075222 |
| 6882 |
1042-1048 |
SequenceVariant |
denotes |
G-395A |
DBSNP:rs1207568 |
| 6883 |
1095-1097 |
DiseaseOrPhenotypicFeature |
denotes |
EH |
MESH:D000075222 |
| 6884 |
1232-1234 |
DiseaseOrPhenotypicFeature |
denotes |
EH |
MESH:D000075222 |
| 6885 |
1242-1247 |
SequenceVariant |
denotes |
-395A |
DBSNP:rs1207568 |
| 6886 |
1426-1431 |
SequenceVariant |
denotes |
-395A |
DBSNP:rs1207568 |
| 6887 |
1481-1487 |
SequenceVariant |
denotes |
G-395A |
DBSNP:rs1207568 |
| 6888 |
1510-1516 |
GeneOrGeneProduct |
denotes |
Klotho |
NCBIGene:9365 |
| 6889 |
1571-1576 |
SequenceVariant |
denotes |
-395G |
DBSNP:rs1207568 |
| 6890 |
1603-1609 |
SequenceVariant |
denotes |
G-395A |
DBSNP:rs1207568 |
| 6891 |
1630-1635 |
OrganismTaxon |
denotes |
human |
NCBITaxon:9606 |
| 6892 |
1636-1642 |
GeneOrGeneProduct |
denotes |
Klotho |
NCBIGene:9365 |
| 6893 |
1667-1669 |
DiseaseOrPhenotypicFeature |
denotes |
EH |
MESH:D000075222 |
