PubMed:17059986 JSONTXT 36 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue ID:
T1 53-70 DiseaseOrPhenotypicFeature denotes Gitelman syndrome D053579
T2 75-111 DiseaseOrPhenotypicFeature denotes idiopathic intracranial hypertension D011559
T3 133-150 DiseaseOrPhenotypicFeature denotes Gitelman syndrome D053579
T4 152-154 DiseaseOrPhenotypicFeature denotes GS D053579
T5 214-226 DiseaseOrPhenotypicFeature denotes growth delay DISEASE
T6 238-247 DiseaseOrPhenotypicFeature denotes alkalosis D000471
T7 249-263 DiseaseOrPhenotypicFeature denotes hypomagnesemia DISEASE
T8 268-279 DiseaseOrPhenotypicFeature denotes hypokalemia D007008
T9 315-351 DiseaseOrPhenotypicFeature denotes idiopathic intracranial hypertension D011559
T10 367-378 DiseaseOrPhenotypicFeature denotes papilledema D010211
T11 380-399 DiseaseOrPhenotypicFeature denotes pseudotumor cerebri D011559
T12 467-499 DiseaseOrPhenotypicFeature denotes cerebral cavernous malformations D020786
T13 546-562 DiseaseOrPhenotypicFeature denotes Bartter syndrome D001477
T14 897-899 DiseaseOrPhenotypicFeature denotes GS D053579
T15 1365-1381 DiseaseOrPhenotypicFeature denotes Bartter syndrome D001477
T16 1382-1384 DiseaseOrPhenotypicFeature denotes GS D053579
T17 1390-1409 DiseaseOrPhenotypicFeature denotes pseudotumor cerebri D011559
T18 1456-1481 DiseaseOrPhenotypicFeature denotes electrolyte abnormalities DISEASE
T19 1496-1509 DiseaseOrPhenotypicFeature denotes aldosteronism D006929
T20 1529-1565 DiseaseOrPhenotypicFeature denotes idiopathic intracranial hypertension D011559
T21 1642-1644 DiseaseOrPhenotypicFeature denotes GS D053579
T22 1750-1773 DiseaseOrPhenotypicFeature denotes familial cavernomatosis DISEASE
T23 1778-1780 DiseaseOrPhenotypicFeature denotes GS D053579