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PubMed:31789978 JSONTXT

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
T0 21-30 REG denotes resulting
T1 34-49 DISEASE denotes nephrolithiasis
T2 83-105 DISEASE denotes pediatric urolithiasi
T3 94-106 DISEASE denotes urolithiasis
T4 262-279 DISEASE denotes metabolic diseas
T5 426-450 DISEASE denotes end-stage kidney diseas
T6 528-549 DISEASE denotes c kidney stone diseas
T7 578-591 DISEASE denotes n hypercalcur
T8 580-593 DISEASE denotes hypercalcuria
T9 638-663 DISEASE denotes f idiopathic hypercalciur
T10 714-744 DISEASE denotes e autosomal recessive heredita
T11 754-761 GENE denotes f CYP24
T12 756-763 GENE denotes CYP24A1
T13 763-770 GENE denotes , SLC34
T14 765-772 GENE denotes SLC34A1
T15 775-782 GENE denotes d SLC34
T16 777-784 GENE denotes SLC34A3
T17 785-795 REG denotes associated
T18 794-823 DISEASE denotes d nephrocalcinosis/urolithias
T19 796-825 DISEASE denotes nephrocalcinosis/urolithiasis
T20 831-839 POSREG denotes elevated
T21 907-913 MPA denotes levels
T22 934-944 POSREG denotes activating
T23 961-970 VAR denotes mutations
T24 978-993 GENE denotes calcium-sensing
T25 1008-1012 REG denotes lead
T26 1020-1022 REG denotes to
T27 1021-1079 DISEASE denotes o hypocalcemic hypercalciuria or hypercalcemic hypocalciur
T28 1023-1050 DISEASE denotes hypocalcemic hypercalciuria
T29 1054-1081 DISEASE denotes hypercalcemic hypocalciuria
T30 1086-1107 DISEASE denotes primary hyperoxaluria
T31 1092-1105 DISEASE denotes y hyperoxalur
T32 1315-1327 DISEASE denotes : Kidney sto
T33 1317-1330 DISEASE denotes Kidney stones
R0 T1 T0 ThemeOf nephrolithiasis,resulting
R1 T19 T17 ThemeOf nephrocalcinosis/urolithiasis,associated
R10 T28 T26 ThemeOf hypocalcemic hypercalciuria,to
R11 T29 T26 ThemeOf hypercalcemic hypocalciuria,to
R2 T19 T20 ThemeOf nephrocalcinosis/urolithiasis,elevated
R3 T21 T20 ThemeOf levels,elevated
R4 T22 T25 CauseOf activating,lead
R5 T22 T26 CauseOf activating,to
R6 T23 T22 CauseOf mutations,activating
R7 T23 T25 CauseOf mutations,lead
R8 T23 T26 CauseOf mutations,to
R9 T24 T23 ThemeOf calcium-sensing,mutations