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PubMed:28728825 JSONTXT

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kaiyin_test

Id Subject Object Predicate Lexical cue
T2 194-210 NegReg denotes Loss-of-function
T3 211-220 Var denotes mutations
T1 234-240 Gene denotes PIEZO1
T21 252-302 Disease denotes autosomal recessive congenital lymphatic dysplasia
T6 304-320 PosReg denotes Gain-of-function
T7 321-330 Var denotes mutations
T5 344-350 Gene denotes PIEZO1
T22 366-401 Disease denotes autosomal dominant hemolytic anemia
T9 403-425 Disease denotes hereditary xerocytosis
T19 441-466 Disease denotes dehydrated stomatocytosis
T11 469-485 NegReg denotes Loss-of-function
T12 486-495 Var denotes mutations
T10 509-515 Gene denotes PIEZO2
T13 530-578 Disease denotes autosomal recessive syndrome of muscular atrophy
T14 616-630 Disease denotes arthrogryposis
T15 636-645 Disease denotes scoliosis
T17 647-663 PosReg denotes Gain-of-function
T18 664-673 Var denotes mutations
T16 687-693 Gene denotes PIEZO2
T20 729-769 Disease denotes autosomal dominant distal arthrogryposis
R1 T1 T3 ThemeOf PIEZO1,mutations
R11 T9 T6 ThemeOf hereditary xerocytosis,Gain-of-function
R12 T19 T6 ThemeOf dehydrated stomatocytosis,Gain-of-function
R13 T13 T11 ThemeOf autosomal recessive syndrome of muscular atrophy,Loss-of-function
R14 T14 T11 ThemeOf arthrogryposis,Loss-of-function
R15 T15 T11 ThemeOf scoliosis,Loss-of-function
R16 T20 T17 ThemeOf autosomal dominant distal arthrogryposis,Gain-of-function
R17 T21 T2 ThemeOf autosomal recessive congenital lymphatic dysplasia,Loss-of-function
R18 T22 T6 ThemeOf autosomal dominant hemolytic anemia,Gain-of-function
R2 T3 T2 CauseOf mutations,Loss-of-function
R3 T5 T7 ThemeOf PIEZO1,mutations
R4 T7 T6 CauseOf mutations,Gain-of-function
R5 T10 T12 ThemeOf PIEZO2,mutations
R6 T12 T11 CauseOf mutations,Loss-of-function
R7 T16 T18 ThemeOf PIEZO2,mutations
R8 T18 T17 CauseOf mutations,Gain-of-function

name_no

Id Subject Object Predicate Lexical cue
T2 194-210 NegReg denotes Loss-of-function
T3 211-220 Var denotes mutations
T1 234-240 Gene denotes PIEZO1
T21 252-302 Disease denotes autosomal recessive congenital lymphatic dysplasia
T6 304-320 PosReg denotes Gain-of-function
T7 321-330 Var denotes mutations
T5 344-350 Gene denotes PIEZO1
T22 366-401 Disease denotes autosomal dominant hemolytic anemia
T9 403-425 Disease denotes hereditary xerocytosis
T19 441-466 Disease denotes dehydrated stomatocytosis
T11 469-485 NegReg denotes Loss-of-function
T12 486-495 Var denotes mutations
T10 509-515 Gene denotes PIEZO2
T13 530-578 Disease denotes autosomal recessive syndrome of muscular atrophy
T14 616-630 Disease denotes arthrogryposis
T15 636-645 Disease denotes scoliosis
T17 647-663 PosReg denotes Gain-of-function
T18 664-673 Var denotes mutations
T16 687-693 Gene denotes PIEZO2
T20 729-769 Disease denotes autosomal dominant distal arthrogryposis
R1 T1 T3 ThemeOf PIEZO1,mutations
R11 T9 T6 ThemeOf hereditary xerocytosis,Gain-of-function
R12 T19 T6 ThemeOf dehydrated stomatocytosis,Gain-of-function
R13 T13 T11 ThemeOf autosomal recessive syndrome of muscular atrophy,Loss-of-function
R14 T14 T11 ThemeOf arthrogryposis,Loss-of-function
R15 T15 T11 ThemeOf scoliosis,Loss-of-function
R16 T20 T17 ThemeOf autosomal dominant distal arthrogryposis,Gain-of-function
R17 T21 T2 ThemeOf autosomal recessive congenital lymphatic dysplasia,Loss-of-function
R18 T22 T6 ThemeOf autosomal dominant hemolytic anemia,Gain-of-function
R2 T3 T2 CauseOf mutations,Loss-of-function
R3 T5 T7 ThemeOf PIEZO1,mutations
R4 T7 T6 CauseOf mutations,Gain-of-function
R5 T10 T12 ThemeOf PIEZO2,mutations
R6 T12 T11 CauseOf mutations,Loss-of-function
R7 T16 T18 ThemeOf PIEZO2,mutations
R8 T18 T17 CauseOf mutations,Gain-of-function