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NCBI-Disease-Corpus-GPT5-withguidelines

Id Subject Object Predicate Lexical cue
T1 54-97 DiseaseClass denotes autosomal dominant cerebellar ataxia type I
T2 259-303 DiseaseClass denotes autosomal dominant cerebellar ataxias type I
T3 305-336 CompositeMention denotes spinocerebellar ataxias 1 and 2
T4 338-342 SpecificDisease denotes SCA1
T5 352-356 SpecificDisease denotes SCA2
T6 370-397 SpecificDisease denotes SCA3/Machado-Joseph disease
T7 399-402 SpecificDisease denotes MJD
T8 417-421 SpecificDisease denotes SCA1
T9 538-542 SpecificDisease denotes SCA2
T10 817-821 SpecificDisease denotes SCA3
T11 1082-1086 SpecificDisease denotes SCA1
T12 1099-1103 SpecificDisease denotes SCA2
T13 1134-1138 SpecificDisease denotes SCA3
T14 1229-1249 CompositeMention denotes SCA1, SCA2, and SCA3

NCBI-Disease-Corpus-GPT5-noguidelines

Id Subject Object Predicate Lexical cue
T1 54-97 DiseaseClass denotes autosomal dominant cerebellar ataxia type I
T2 259-303 DiseaseClass denotes autosomal dominant cerebellar ataxias type I
T3 305-336 CompositeMention denotes spinocerebellar ataxias 1 and 2
T4 338-342 SpecificDisease denotes SCA1
T5 352-356 SpecificDisease denotes SCA2
T6 370-403 SpecificDisease denotes SCA3/Machado-Joseph disease (MJD)
T7 417-421 SpecificDisease denotes SCA1
T8 538-542 SpecificDisease denotes SCA2
T9 817-821 SpecificDisease denotes SCA3
T10 1082-1086 SpecificDisease denotes SCA1
T11 1099-1103 SpecificDisease denotes SCA2
T12 1134-1138 SpecificDisease denotes SCA3
T13 1229-1249 CompositeMention denotes SCA1, SCA2, and SCA3

NCBI-Disease-Corpus-GPT5-guidelineprompt

Id Subject Object Predicate Lexical cue
T1 54-97 DiseaseClass denotes autosomal dominant cerebellar ataxia type I
T2 259-303 DiseaseClass denotes autosomal dominant cerebellar ataxias type I
T3 305-336 CompositeMention denotes spinocerebellar ataxias 1 and 2
T4 338-342 SpecificDisease denotes SCA1
T5 352-356 SpecificDisease denotes SCA2
T6 370-397 SpecificDisease denotes SCA3/Machado-Joseph disease
T7 399-402 SpecificDisease denotes MJD
T8 417-421 SpecificDisease denotes SCA1
T9 538-542 SpecificDisease denotes SCA2
T10 817-821 SpecificDisease denotes SCA3
T11 1082-1086 SpecificDisease denotes SCA1
T12 1099-1103 SpecificDisease denotes SCA2
T13 1134-1138 SpecificDisease denotes SCA3
T14 1229-1249 CompositeMention denotes SCA1, SCA2, and SCA3

NCBI-Disease-Corpus-Moderated1

Id Subject Object Predicate Lexical cue
T1 54-97 DiseaseClass denotes autosomal dominant cerebellar ataxia type I
T2 259-303 DiseaseClass denotes autosomal dominant cerebellar ataxias type I
T3 305-336 CompositeMention denotes spinocerebellar ataxias 1 and 2
T4 338-342 SpecificDisease denotes SCA1
T5 352-356 SpecificDisease denotes SCA2
T6 370-374 SpecificDisease denotes SCA3
T7 375-397 SpecificDisease denotes Machado-Joseph disease
T8 399-402 SpecificDisease denotes MJD
T9 417-421 SpecificDisease denotes SCA1
T10 538-542 SpecificDisease denotes SCA2
T11 817-821 SpecificDisease denotes SCA3
T12 1082-1086 SpecificDisease denotes SCA1
T13 1099-1103 SpecificDisease denotes SCA2
T14 1134-1138 SpecificDisease denotes SCA3
T15 1229-1233 SpecificDisease denotes SCA1
T16 1235-1239 SpecificDisease denotes SCA2
T17 1245-1249 SpecificDisease denotes SCA3

DisGeNET

Id Subject Object Predicate Lexical cue
T0 1245-1249 gene:4287 denotes SCA3
T1 1012-1033 disease:C0271390 denotes gaze-evoked nystagmus
R1 T0 T1 associated_with SCA3,gaze-evoked nystagmus

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
9506545-1#239#243#gene6310 338-342 gene6310 denotes SCA1
9506545-1#179#197#diseaseC0007758 278-296 diseaseC0007758 denotes cerebellar ataxias
9506545-7#308#312#gene4287 1245-1249 gene4287 denotes SCA3
9506545-7#75#96#diseaseC0271390 1012-1033 diseaseC0271390 denotes gaze-evoked nystagmus
239#243#gene6310179#197#diseaseC0007758 9506545-1#239#243#gene6310 9506545-1#179#197#diseaseC0007758 associated_with SCA1,cerebellar ataxias
308#312#gene428775#96#diseaseC0271390 9506545-7#308#312#gene4287 9506545-7#75#96#diseaseC0271390 associated_with SCA3,gaze-evoked nystagmus

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 0-26 DiseaseClass:D005124 denotes Eye movement abnormalities
T2 73-97 DiseaseClass:D020754 denotes cerebellar ataxia type I
T3 278-303 DiseaseClass:D020754 denotes cerebellar ataxias type I
T4 305-336 CompositeMention:OMIM:164400|OMIM:183090 denotes spinocerebellar ataxias 1 and 2
T5 338-342 SpecificDisease:OMIM:164400 denotes SCA1
T6 352-356 SpecificDisease:OMIM:183090 denotes SCA2
T7 370-374 SpecificDisease:D017827 denotes SCA3
T8 375-397 SpecificDisease:D017827 denotes Machado-Joseph disease
T9 399-402 SpecificDisease:D017827 denotes MJD
T10 417-421 SpecificDisease:OMIM:164400 denotes SCA1
T11 483-494 SpecificDisease:D002524 denotes hypermetria
T12 538-542 SpecificDisease:OMIM:183090 denotes SCA2
T13 817-821 SpecificDisease:D017827 denotes SCA3
T14 823-844 SpecificDisease:D009759 denotes gaze-evoked nystagmus
T15 1012-1033 SpecificDisease:D009759 denotes gaze-evoked nystagmus
T16 1082-1086 SpecificDisease:OMIM:164400 denotes SCA1
T17 1099-1103 SpecificDisease:OMIM:183090 denotes SCA2
T18 1134-1138 SpecificDisease:D017827 denotes SCA3
T19 1229-1233 SpecificDisease:OMIM:164400 denotes SCA1
T20 1235-1239 SpecificDisease:OMIM:183090 denotes SCA2
T21 1245-1249 SpecificDisease:D017827 denotes SCA3

NCBI-Disease-Test

Id Subject Object Predicate Lexical cue database_id
T290 0-26 DiseaseClass denotes Eye movement abnormalities D005124
T291 73-97 DiseaseClass denotes cerebellar ataxia type I D020754
T292 278-303 DiseaseClass denotes cerebellar ataxias type I D020754
T293 305-336 CompositeMention denotes spinocerebellar ataxias 1 and 2 OMIM:164400|OMIM:183090
T294 338-342 SpecificDisease denotes SCA1 OMIM:164400
T295 352-356 SpecificDisease denotes SCA2 OMIM:183090
T296 370-374 SpecificDisease denotes SCA3 D017827
T297 375-397 SpecificDisease denotes Machado-Joseph disease D017827
T298 399-402 SpecificDisease denotes MJD D017827
T299 417-421 SpecificDisease denotes SCA1 OMIM:164400
T300 483-494 SpecificDisease denotes hypermetria D002524
T301 538-542 SpecificDisease denotes SCA2 OMIM:183090
T302 817-821 SpecificDisease denotes SCA3 D017827
T303 823-844 SpecificDisease denotes gaze-evoked nystagmus D009759
T304 1012-1033 SpecificDisease denotes gaze-evoked nystagmus D009759
T305 1082-1086 SpecificDisease denotes SCA1 OMIM:164400
T306 1099-1103 SpecificDisease denotes SCA2 OMIM:183090
T307 1134-1138 SpecificDisease denotes SCA3 D017827
T308 1229-1233 SpecificDisease denotes SCA1 OMIM:164400
T309 1235-1239 SpecificDisease denotes SCA2 OMIM:183090
T310 1245-1249 SpecificDisease denotes SCA3 D017827

NCBI-Disease-Test-Assistant-Knowledge

Id Subject Object Predicate Lexical cue
T1 54-97 DiseaseClass denotes autosomal dominant cerebellar ataxia type I
T2 259-303 DiseaseClass denotes autosomal dominant cerebellar ataxias type I
T3 305-330 SpecificDisease denotes spinocerebellar ataxias 1
T4 335-336 SpecificDisease denotes 2
T5 338-342 SpecificDisease denotes SCA1
T6 352-356 SpecificDisease denotes SCA2
T7 370-397 CompositeMention denotes SCA3/Machado-Joseph disease
T8 417-421 SpecificDisease denotes SCA1
T9 538-542 SpecificDisease denotes SCA2
T10 817-821 SpecificDisease denotes SCA3
T11 1082-1086 SpecificDisease denotes SCA1
T12 1099-1103 SpecificDisease denotes SCA2
T13 1134-1138 SpecificDisease denotes SCA3
T14 1229-1233 SpecificDisease denotes SCA1
T15 1235-1239 SpecificDisease denotes SCA2
T16 1245-1249 SpecificDisease denotes SCA3

NCBI-Disease-Test-4o-NoGuidelineInPrompt

Id Subject Object Predicate Lexical cue
T1 54-97 SpecificDisease denotes autosomal dominant cerebellar ataxia type I
T2 259-303 DiseaseClass denotes autosomal dominant cerebellar ataxias type I
T3 305-330 SpecificDisease denotes spinocerebellar ataxias 1
T4 335-336 SpecificDisease denotes 2
T5 370-397 CompositeMention denotes SCA3/Machado-Joseph disease
T6 417-421 SpecificDisease denotes SCA1
T7 483-494 Modifier denotes hypermetria
T8 538-542 SpecificDisease denotes SCA2
T9 693-706 Modifier denotes disease onset
T10 817-821 SpecificDisease denotes SCA3
T11 823-844 Modifier denotes gaze-evoked nystagmus
T12 878-888 Modifier denotes hypometria
T13 1012-1033 Modifier denotes gaze-evoked nystagmus
T14 1082-1086 SpecificDisease denotes SCA1
T15 1099-1103 SpecificDisease denotes SCA2
T16 1134-1138 SpecificDisease denotes SCA3
T17 1229-1233 SpecificDisease denotes SCA1
T18 1235-1239 SpecificDisease denotes SCA2
T19 1245-1249 SpecificDisease denotes SCA3
T20 1282-1290 DiseaseClass denotes diseases

NCBI-Disease-Corpus-o3-2

Id Subject Object Predicate Lexical cue
T1 54-97 DiseaseClass denotes autosomal dominant cerebellar ataxia type I
T2 259-303 DiseaseClass denotes autosomal dominant cerebellar ataxias type I
T3 305-336 CompositeMention denotes spinocerebellar ataxias 1 and 2
T4 338-342 SpecificDisease denotes SCA1
T5 352-356 SpecificDisease denotes SCA2
T6 370-397 SpecificDisease denotes SCA3/Machado-Joseph disease
T7 417-421 SpecificDisease denotes SCA1
T8 538-542 SpecificDisease denotes SCA2
T9 817-821 SpecificDisease denotes SCA3
T10 1082-1086 SpecificDisease denotes SCA1
T11 1099-1103 SpecificDisease denotes SCA2
T12 1134-1138 SpecificDisease denotes SCA3
T13 1229-1233 SpecificDisease denotes SCA1
T14 1235-1239 SpecificDisease denotes SCA2
T15 1245-1249 SpecificDisease denotes SCA3

NCBI-Disease-Corpus-high-o3-1

Id Subject Object Predicate Lexical cue
T1 54-97 SpecificDisease denotes autosomal dominant cerebellar ataxia type I
T2 259-303 SpecificDisease denotes autosomal dominant cerebellar ataxias type I
T3 305-330 SpecificDisease denotes spinocerebellar ataxias 1
T4 311-336 SpecificDisease denotes erebellar ataxias 1 and 2
T5 338-342 SpecificDisease denotes SCA1
T6 352-356 SpecificDisease denotes SCA2
T7 370-374 CompositeMention denotes SCA3
T8 375-397 CompositeMention denotes Machado-Joseph disease
T9 399-402 CompositeMention denotes MJD
T10 417-421 SpecificDisease denotes SCA1
T11 538-542 SpecificDisease denotes SCA2
T12 817-821 SpecificDisease denotes SCA3
T13 1082-1086 SpecificDisease denotes SCA1
T14 1099-1103 SpecificDisease denotes SCA2
T15 1134-1138 SpecificDisease denotes SCA3
T16 1229-1233 SpecificDisease denotes SCA1
T17 1235-1239 SpecificDisease denotes SCA2
T18 1245-1249 SpecificDisease denotes SCA3

NCBI-Disease-Corpus-high-o3-2

Id Subject Object Predicate Lexical cue
T1 54-97 DiseaseClass denotes autosomal dominant cerebellar ataxia type I
T2 259-303 DiseaseClass denotes autosomal dominant cerebellar ataxias type I
T5 338-342 SpecificDisease denotes SCA1
T6 352-356 SpecificDisease denotes SCA2
T7 370-374 CompositeMention denotes SCA3
T8 375-397 CompositeMention denotes Machado-Joseph disease
T9 399-402 SpecificDisease denotes MJD
T10 417-421 SpecificDisease denotes SCA1
T11 538-542 SpecificDisease denotes SCA2
T12 817-821 SpecificDisease denotes SCA3
T13 1082-1086 SpecificDisease denotes SCA1
T14 1099-1103 SpecificDisease denotes SCA2
T15 1134-1138 SpecificDisease denotes SCA3
T16 1229-1233 SpecificDisease denotes SCA1
T17 1235-1239 SpecificDisease denotes SCA2
T18 1245-1249 SpecificDisease denotes SCA3

NCBI-Disease-Test-4o-GuidelineInPrompt

Id Subject Object Predicate Lexical cue
T1 54-97 DiseaseClass denotes autosomal dominant cerebellar ataxia type I
T2 259-303 DiseaseClass denotes autosomal dominant cerebellar ataxias type I
T3 305-330 SpecificDisease denotes spinocerebellar ataxias 1
T4 335-336 SpecificDisease denotes 2
T5 338-342 SpecificDisease denotes SCA1
T6 352-356 SpecificDisease denotes SCA2
T7 370-397 SpecificDisease denotes SCA3/Machado-Joseph disease
T8 417-421 SpecificDisease denotes SCA1
T9 538-542 SpecificDisease denotes SCA2
T10 817-821 SpecificDisease denotes SCA3
T11 1082-1086 SpecificDisease denotes SCA1
T12 1099-1103 SpecificDisease denotes SCA2
T13 1134-1138 SpecificDisease denotes SCA3
T14 1229-1233 SpecificDisease denotes SCA1
T15 1235-1239 SpecificDisease denotes SCA2
T16 1245-1249 SpecificDisease denotes SCA3

NCBI-Disease-Corpus-UpdatedGuideline

Id Subject Object Predicate Lexical cue
T1 54-97 DiseaseClass denotes autosomal dominant cerebellar ataxia type I
T2 259-303 DiseaseClass denotes autosomal dominant cerebellar ataxias type I
T3 305-336 CompositeMention denotes spinocerebellar ataxias 1 and 2
T4 338-342 SpecificDisease denotes SCA1
T5 352-356 SpecificDisease denotes SCA2
T6 370-397 CompositeMention denotes SCA3/Machado-Joseph disease
T7 399-402 SpecificDisease denotes MJD
T8 417-421 SpecificDisease denotes SCA1
T9 538-542 SpecificDisease denotes SCA2
T10 817-821 SpecificDisease denotes SCA3
T11 1082-1086 SpecificDisease denotes SCA1
T12 1099-1103 SpecificDisease denotes SCA2
T13 1134-1138 SpecificDisease denotes SCA3
T14 1229-1233 SpecificDisease denotes SCA1
T15 1235-1239 SpecificDisease denotes SCA2
T16 1245-1249 SpecificDisease denotes SCA3

NCBI-Disease-Corpus-humanintheloop

Id Subject Object Predicate Lexical cue
T1 54-97 DiseaseClass denotes autosomal dominant cerebellar ataxia type I
T2 259-303 DiseaseClass denotes autosomal dominant cerebellar ataxias type I
T3 305-330 SpecificDisease denotes spinocerebellar ataxias 1
T4 335-336 SpecificDisease denotes 2
T5 338-342 SpecificDisease denotes SCA1
T6 352-356 SpecificDisease denotes SCA2
T7 370-397 CompositeMention denotes SCA3/Machado-Joseph disease
T8 399-402 SpecificDisease denotes MJD
T9 417-421 SpecificDisease denotes SCA1
T10 538-542 SpecificDisease denotes SCA2
T11 817-821 SpecificDisease denotes SCA3
T12 1082-1086 SpecificDisease denotes SCA1
T13 1099-1103 SpecificDisease denotes SCA2
T14 1134-1138 SpecificDisease denotes SCA3
T15 1229-1233 SpecificDisease denotes SCA1
T16 1235-1239 SpecificDisease denotes SCA2
T17 1245-1249 SpecificDisease denotes SCA3

NCBI-Disease-Corpus-rezarta1

Id Subject Object Predicate Lexical cue
T1 54-97 DiseaseClass denotes autosomal dominant cerebellar ataxia type I
T2 259-303 DiseaseClass denotes autosomal dominant cerebellar ataxias type I
T3 305-330 SpecificDisease denotes spinocerebellar ataxias 1
T4 335-336 SpecificDisease denotes 2
T5 338-342 SpecificDisease denotes SCA1
T6 352-356 SpecificDisease denotes SCA2
T7 370-397 SpecificDisease denotes SCA3/Machado-Joseph disease
T8 399-402 SpecificDisease denotes MJD
T9 417-421 SpecificDisease denotes SCA1
T10 538-542 SpecificDisease denotes SCA2
T11 817-821 SpecificDisease denotes SCA3
T12 1082-1086 SpecificDisease denotes SCA1
T13 1099-1103 SpecificDisease denotes SCA2
T14 1134-1138 SpecificDisease denotes SCA3
T15 1229-1233 SpecificDisease denotes SCA1
T16 1235-1239 SpecificDisease denotes SCA2
T17 1245-1249 SpecificDisease denotes SCA3

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T290 0-26 DiseaseClass denotes Eye movement abnormalities D005124
T291 73-97 DiseaseClass denotes cerebellar ataxia type I D020754
T292 278-303 DiseaseClass denotes cerebellar ataxias type I D020754
T293 305-336 CompositeMention denotes spinocerebellar ataxias 1 and 2 OMIM:164400|OMIM:183090
T294 338-342 SpecificDisease denotes SCA1 OMIM:164400
T295 352-356 SpecificDisease denotes SCA2 OMIM:183090
T296 370-374 SpecificDisease denotes SCA3 D017827
T297 375-397 SpecificDisease denotes Machado-Joseph disease D017827
T298 399-402 SpecificDisease denotes MJD D017827
T299 417-421 SpecificDisease denotes SCA1 OMIM:164400
T300 483-494 SpecificDisease denotes hypermetria D002524
T301 538-542 SpecificDisease denotes SCA2 OMIM:183090
T302 817-821 SpecificDisease denotes SCA3 D017827
T303 823-844 SpecificDisease denotes gaze-evoked nystagmus D009759
T304 1012-1033 SpecificDisease denotes gaze-evoked nystagmus D009759
T305 1082-1086 SpecificDisease denotes SCA1 OMIM:164400
T306 1099-1103 SpecificDisease denotes SCA2 OMIM:183090
T307 1134-1138 SpecificDisease denotes SCA3 D017827
T308 1229-1233 SpecificDisease denotes SCA1 OMIM:164400
T309 1235-1239 SpecificDisease denotes SCA2 OMIM:183090
T310 1245-1249 SpecificDisease denotes SCA3 D017827

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 54-97 SpecificDisease denotes autosomal dominant cerebellar ataxia type I
T2 259-303 DiseaseClass denotes autosomal dominant cerebellar ataxias type I
T3 305-330 SpecificDisease denotes spinocerebellar ataxias 1
T4 335-336 SpecificDisease denotes 2
T5 338-342 SpecificDisease denotes SCA1
T6 352-356 SpecificDisease denotes SCA2
T7 370-374 SpecificDisease denotes SCA3
T8 375-397 SpecificDisease denotes Machado-Joseph disease
T9 399-402 SpecificDisease denotes MJD
T10 417-421 SpecificDisease denotes SCA1
T11 538-542 SpecificDisease denotes SCA2
T12 817-821 SpecificDisease denotes SCA3
T13 1082-1086 SpecificDisease denotes SCA1
T14 1099-1103 SpecificDisease denotes SCA2
T15 1134-1138 SpecificDisease denotes SCA3
T16 1229-1233 SpecificDisease denotes SCA1
T17 1235-1239 SpecificDisease denotes SCA2
T18 1245-1249 SpecificDisease denotes SCA3

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 54-97 SpecificDisease denotes autosomal dominant cerebellar ataxia type I
T2 259-303 DiseaseClass denotes autosomal dominant cerebellar ataxias type I
T3 305-330 SpecificDisease denotes spinocerebellar ataxias 1
T4 335-336 SpecificDisease denotes 2
T5 338-342 Modifier denotes SCA1
T6 352-356 Modifier denotes SCA2
T7 370-397 CompositeMention denotes SCA3/Machado-Joseph disease
T8 399-402 Modifier denotes MJD
T9 417-421 SpecificDisease denotes SCA1
T10 538-542 SpecificDisease denotes SCA2
T11 817-821 SpecificDisease denotes SCA3
T12 1082-1086 SpecificDisease denotes SCA1
T13 1099-1103 SpecificDisease denotes SCA2
T14 1134-1138 SpecificDisease denotes SCA3
T15 1229-1233 Modifier denotes SCA1
T16 1235-1239 Modifier denotes SCA2
T17 1245-1249 Modifier denotes SCA3

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 54-97 DiseaseClass denotes autosomal dominant cerebellar ataxia type I
T2 259-303 DiseaseClass denotes autosomal dominant cerebellar ataxias type I
T3 305-330 SpecificDisease denotes spinocerebellar ataxias 1
T4 335-336 SpecificDisease denotes 2
T5 370-397 SpecificDisease denotes SCA3/Machado-Joseph disease
T6 417-421 Modifier denotes SCA1
T7 538-542 Modifier denotes SCA2
T8 817-821 Modifier denotes SCA3
T9 1082-1086 Modifier denotes SCA1
T10 1099-1103 Modifier denotes SCA2
T11 1134-1138 Modifier denotes SCA3
T12 1229-1233 SpecificDisease denotes SCA1
T13 1235-1239 SpecificDisease denotes SCA2
T14 1245-1249 SpecificDisease denotes SCA3

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 0-26 DiseaseClass denotes Eye movement abnormalities
T2 54-97 SpecificDisease denotes autosomal dominant cerebellar ataxia type I
T3 259-303 DiseaseClass denotes autosomal dominant cerebellar ataxias type I
T4 305-336 SpecificDisease denotes spinocerebellar ataxias 1 and 2
T5 338-342 SpecificDisease denotes SCA1
T6 352-356 SpecificDisease denotes SCA2
T7 370-403 CompositeMention denotes SCA3/Machado-Joseph disease (MJD)
T8 417-421 SpecificDisease denotes SCA1
T9 483-494 DiseaseClass denotes hypermetria
T10 538-542 SpecificDisease denotes SCA2
T11 693-706 CompositeMention denotes disease onset
T12 817-821 SpecificDisease denotes SCA3
T13 1082-1086 SpecificDisease denotes SCA1
T14 1099-1103 SpecificDisease denotes SCA2
T15 1134-1138 SpecificDisease denotes SCA3
T16 1229-1233 SpecificDisease denotes SCA1
T17 1235-1239 SpecificDisease denotes SCA2
T18 1245-1249 SpecificDisease denotes SCA3
T19 1282-1291 CompositeMention denotes diseases.

123456

Id Subject Object Predicate Lexical cue
T1 54-97 DiseaseClass denotes autosomal dominant cerebellar ataxia type I
T2 259-303 DiseaseClass denotes autosomal dominant cerebellar ataxias type I
T3 305-330 SpecificDisease denotes spinocerebellar ataxias 1
T4 335-336 SpecificDisease denotes 2
T5 338-342 SpecificDisease denotes SCA1
T6 352-356 SpecificDisease denotes SCA2
T7 370-397 CompositeMention denotes SCA3/Machado-Joseph disease
T8 399-402 SpecificDisease denotes MJD
T9 417-421 SpecificDisease denotes SCA1
T10 538-542 SpecificDisease denotes SCA2
T11 817-821 SpecificDisease denotes SCA3
T12 1082-1086 SpecificDisease denotes SCA1
T13 1099-1103 SpecificDisease denotes SCA2
T14 1134-1138 SpecificDisease denotes SCA3
T15 1229-1233 SpecificDisease denotes SCA1
T16 1235-1239 SpecificDisease denotes SCA2
T17 1245-1249 SpecificDisease denotes SCA3

12345

Id Subject Object Predicate Lexical cue
T1 54-97 DiseaseClass denotes autosomal dominant cerebellar ataxia type I
T2 259-303 DiseaseClass denotes autosomal dominant cerebellar ataxias type I
T3 305-336 CompositeMention denotes spinocerebellar ataxias 1 and 2
T4 338-342 SpecificDisease denotes SCA1
T5 352-356 SpecificDisease denotes SCA2
T6 370-397 CompositeMention denotes SCA3/Machado-Joseph disease
T7 399-402 SpecificDisease denotes MJD
T8 417-421 SpecificDisease denotes SCA1
T9 538-542 SpecificDisease denotes SCA2
T10 817-821 SpecificDisease denotes SCA3
T11 1082-1086 SpecificDisease denotes SCA1
T12 1099-1103 SpecificDisease denotes SCA2
T13 1134-1138 SpecificDisease denotes SCA3
T14 1229-1233 SpecificDisease denotes SCA1
T15 1235-1239 SpecificDisease denotes SCA2
T16 1245-1249 SpecificDisease denotes SCA3