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PubMed:23956106 JSONTXT 12 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
T0 23-41 DISEASE denotes achondrogenesis 1A
T1 23-41 GENE denotes achondrogenesis 1A
T2 43-61 DISEASE denotes Achondrogenesis 1A
T3 43-61 GENE denotes Achondrogenesis 1A
T4 63-68 DISEASE denotes ACG1A
T5 63-68 GENE denotes ACG1A
T6 128-146 CPA denotes skeletal dysplasia
T7 128-146 DISEASE denotes skeletal dysplasia
T8 158-185 CPA denotes intrauterine growth failure
T9 158-185 DISEASE denotes intrauterine growth failure
T10 187-197 CPA denotes micromelia
T11 199-221 CPA denotes minor facial anomalies
T12 205-221 DISEASE denotes facial anomalies
T13 223-232 NEGREG denotes deficient
T14 233-245 CPA denotes ossification
T15 260-266 NEGREG denotes absent
T16 280-309 CPA denotes defective spinal ossification
T17 311-328 CPA denotes short beaded ribs
T18 334-359 CPA denotes short deformed long bones
T19 367-386 CPA denotes stellate appearance
T20 388-393 DISEASE denotes ACG1A
T21 388-393 GENE denotes ACG1A
T22 397-403 REG denotes caused
T23 407-416 VAR denotes mutations
T24 424-430 GENE denotes TRIP11
T25 437-446 REG denotes resulting
T26 450-460 NEGREG denotes deficiency
T27 450-485 DISEASE denotes deficiency of the Golgi microtubule
T28 505-508 GENE denotes 210
T29 598-603 DISEASE denotes ACG1A
T30 598-603 GENE denotes ACG1A
T31 636-653 VAR denotes nonsense mutation
T32 661-667 GENE denotes TRIP11
T33 780-806 CPA denotes lethal skeletal dysplasias
T34 787-806 DISEASE denotes skeletal dysplasias
T35 854-871 VAR denotes nonsense mutation
T36 878-886 VAR denotes deletion
T37 908-914 GENE denotes TRIP11
T38 938-947 VAR denotes mutations
T39 955-961 GENE denotes TRIP11
T40 971-980 REG denotes encompass
R0 T2 T6 ThemeOf Achondrogenesis 1A,skeletal dysplasia
R1 T4 T6 ThemeOf ACG1A,skeletal dysplasia
R10 T20 T22 ThemeOf ACG1A,caused
R11 T23 T22 CauseOf mutations,caused
R12 T23 T25 CauseOf mutations,resulting
R13 T23 T26 CauseOf mutations,deficiency
R14 T24 T23 ThemeOf TRIP11,mutations
R15 T26 T25 CauseOf deficiency,resulting
R16 T28 T26 ThemeOf 210,deficiency
R17 T32 T31 ThemeOf TRIP11,nonsense mutation
R18 T35 T33 CauseOf nonsense mutation,lethal skeletal dysplasias
R19 T36 T33 CauseOf deletion,lethal skeletal dysplasias
R2 T8 T6 ThemeOf intrauterine growth failure,skeletal dysplasia
R20 T37 T35 ThemeOf TRIP11,nonsense mutation
R21 T37 T36 ThemeOf TRIP11,deletion
R22 T37 T38 ThemeOf TRIP11,mutations
R23 T38 T40 CauseOf mutations,encompass
R24 T39 T35 ThemeOf TRIP11,nonsense mutation
R25 T39 T36 ThemeOf TRIP11,deletion
R26 T39 T38 ThemeOf TRIP11,mutations
R3 T10 T6 ThemeOf micromelia,skeletal dysplasia
R4 T11 T6 ThemeOf minor facial anomalies,skeletal dysplasia
R5 T14 T6 ThemeOf ossification,skeletal dysplasia
R6 T16 T6 ThemeOf defective spinal ossification,skeletal dysplasia
R7 T17 T6 ThemeOf short beaded ribs,skeletal dysplasia
R8 T18 T6 ThemeOf short deformed long bones,skeletal dysplasia
R9 T19 T6 ThemeOf stellate appearance,skeletal dysplasia