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PubMed:9668171 JSONTXT

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NCBI-Disease-Corpus-GPT5-withguidelines

Id Subject Object Predicate Lexical cue
T1 65-83 Modifier denotes myotonic dystrophy
T2 267-269 Modifier denotes DM
T3 326-344 SpecificDisease denotes myotonic dystrophy
T4 346-348 SpecificDisease denotes DM
T5 650-652 SpecificDisease denotes DM
T6 669-685 DiseaseClass denotes genetic diseases
T7 880-882 Modifier denotes DM
T8 1166-1168 Modifier denotes DM

NCBI-Disease-Corpus-GPT5-noguidelines

Id Subject Object Predicate Lexical cue
T1 65-83 SpecificDisease denotes myotonic dystrophy
T2 326-344 SpecificDisease denotes myotonic dystrophy
T3 346-348 SpecificDisease denotes DM
T4 650-652 SpecificDisease denotes DM
T5 663-685 DiseaseClass denotes human genetic diseases
T6 880-882 SpecificDisease denotes DM
T7 1166-1168 SpecificDisease denotes DM

NCBI-Disease-Corpus-GPT5-guidelineprompt

Id Subject Object Predicate Lexical cue
T1 65-83 Modifier denotes myotonic dystrophy
T2 267-269 Modifier denotes DM
T3 326-344 SpecificDisease denotes myotonic dystrophy
T4 346-348 SpecificDisease denotes DM
T5 650-652 SpecificDisease denotes DM
T6 669-685 DiseaseClass denotes genetic diseases
T7 880-882 Modifier denotes DM
T8 1166-1168 Modifier denotes DM

NCBI-Disease-Corpus-Moderated1

Id Subject Object Predicate Lexical cue
T1 65-83 Modifier denotes myotonic dystrophy
T2 267-269 Modifier denotes DM
T3 326-344 SpecificDisease denotes myotonic dystrophy
T4 346-348 SpecificDisease denotes DM
T5 650-652 SpecificDisease denotes DM
T6 663-685 DiseaseClass denotes human genetic diseases
T7 880-882 Modifier denotes DM
T8 1166-1168 Modifier denotes DM

DisGeNET

Id Subject Object Predicate Lexical cue
T0 267-284 gene:1760 denotes DM protein kinase
T1 326-344 disease:C0410226 denotes myotonic dystrophy
T2 267-284 gene:1760 denotes DM protein kinase
T3 326-344 disease:C0027126 denotes myotonic dystrophy
T4 267-284 gene:1760 denotes DM protein kinase
T5 346-348 disease:C0410226 denotes DM
T6 267-284 gene:1760 denotes DM protein kinase
T7 346-348 disease:C0027126 denotes DM
T8 292-296 gene:1760 denotes DMPK
T9 326-344 disease:C0410226 denotes myotonic dystrophy
T10 292-296 gene:1760 denotes DMPK
T11 326-344 disease:C0027126 denotes myotonic dystrophy
T12 292-296 gene:1760 denotes DMPK
T13 346-348 disease:C0410226 denotes DM
T14 292-296 gene:1760 denotes DMPK
T15 346-348 disease:C0027126 denotes DM
R1 T0 T1 associated_with DM protein kinase,myotonic dystrophy
R2 T2 T3 associated_with DM protein kinase,myotonic dystrophy
R3 T4 T5 associated_with DM protein kinase,DM
R4 T6 T7 associated_with DM protein kinase,DM
R5 T8 T9 associated_with DMPK,myotonic dystrophy
R6 T10 T11 associated_with DMPK,myotonic dystrophy
R7 T12 T13 associated_with DMPK,DM
R8 T14 T15 associated_with DMPK,DM

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
9668171-1#61#78#gene1760 267-284 gene1760 denotes DM protein kinase
9668171-1#86#90#gene1760 292-296 gene1760 denotes DMPK
9668171-1#120#138#diseaseC0027126 326-344 diseaseC0027126 denotes myotonic dystrophy
9668171-1#140#142#diseaseC0027126 346-348 diseaseC0027126 denotes DM
9668171-1#120#138#diseaseC0027126 326-344 diseaseC0027126 denotes myotonic dystrophy
9668171-1#140#142#diseaseC0027126 346-348 diseaseC0027126 denotes DM
61#78#gene1760120#138#diseaseC0027126 9668171-1#61#78#gene1760 9668171-1#120#138#diseaseC0027126 associated_with DM protein kinase,myotonic dystrophy
61#78#gene1760140#142#diseaseC0027126 9668171-1#61#78#gene1760 9668171-1#140#142#diseaseC0027126 associated_with DM protein kinase,DM
61#78#gene1760120#138#diseaseC0027126 9668171-1#61#78#gene1760 9668171-1#120#138#diseaseC0027126 associated_with DM protein kinase,myotonic dystrophy
61#78#gene1760140#142#diseaseC0027126 9668171-1#61#78#gene1760 9668171-1#140#142#diseaseC0027126 associated_with DM protein kinase,DM
86#90#gene1760120#138#diseaseC0027126 9668171-1#86#90#gene1760 9668171-1#120#138#diseaseC0027126 associated_with DMPK,myotonic dystrophy
86#90#gene1760140#142#diseaseC0027126 9668171-1#86#90#gene1760 9668171-1#140#142#diseaseC0027126 associated_with DMPK,DM
86#90#gene1760120#138#diseaseC0027126 9668171-1#86#90#gene1760 9668171-1#120#138#diseaseC0027126 associated_with DMPK,myotonic dystrophy
86#90#gene1760140#142#diseaseC0027126 9668171-1#86#90#gene1760 9668171-1#140#142#diseaseC0027126 associated_with DMPK,DM

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 65-83 Modifier:D009223 denotes myotonic dystrophy
T2 326-344 SpecificDisease:D009223 denotes myotonic dystrophy
T3 346-348 SpecificDisease:D009223 denotes DM
T4 650-652 SpecificDisease:D009223 denotes DM
T5 669-685 DiseaseClass:D030342 denotes genetic diseases
T6 880-882 Modifier:D009223 denotes DM
T7 1166-1168 Modifier:D009223 denotes DM

NCBI-Disease-Test

Id Subject Object Predicate Lexical cue database_id
T117 65-83 Modifier denotes myotonic dystrophy D009223
T118 326-344 SpecificDisease denotes myotonic dystrophy D009223
T119 346-348 SpecificDisease denotes DM D009223
T120 650-652 SpecificDisease denotes DM D009223
T121 669-685 DiseaseClass denotes genetic diseases D030342
T122 880-882 Modifier denotes DM D009223
T123 1166-1168 Modifier denotes DM D009223

NCBI-Disease-Test-Assistant-Knowledge

Id Subject Object Predicate Lexical cue
T1 65-83 SpecificDisease denotes myotonic dystrophy
T2 326-349 SpecificDisease denotes myotonic dystrophy (DM)
T3 650-652 SpecificDisease denotes DM
T4 663-685 DiseaseClass denotes human genetic diseases
T5 880-882 SpecificDisease denotes DM
T6 1166-1168 SpecificDisease denotes DM

NCBI-Disease-Test-4o-NoGuidelineInPrompt

Id Subject Object Predicate Lexical cue
T1 65-83 SpecificDisease denotes myotonic dystrophy
T2 326-349 SpecificDisease denotes myotonic dystrophy (DM)
T3 470-478 Modifier denotes patients
T4 650-652 SpecificDisease denotes DM
T5 657-685 DiseaseClass denotes other human genetic diseases
T6 880-882 SpecificDisease denotes DM
T7 1166-1168 SpecificDisease denotes DM
T8 1169-1177 Modifier denotes patients

NCBI-Disease-Corpus-o3-2

Id Subject Object Predicate Lexical cue
T1 65-83 Modifier denotes myotonic dystrophy
T2 326-344 SpecificDisease denotes myotonic dystrophy
T3 346-348 SpecificDisease denotes DM
T4 650-652 SpecificDisease denotes DM
T5 657-685 DiseaseClass denotes other human genetic diseases
T6 880-882 Modifier denotes DM
T7 1166-1168 Modifier denotes DM

NCBI-Disease-Corpus-high-o3-1

Id Subject Object Predicate Lexical cue
T1 65-83 SpecificDisease denotes myotonic dystrophy
T2 326-344 SpecificDisease denotes myotonic dystrophy
T3 346-348 SpecificDisease denotes DM
T4 650-652 SpecificDisease denotes DM
T5 880-882 SpecificDisease denotes DM
T6 1166-1168 SpecificDisease denotes DM

NCBI-Disease-Corpus-high-o3-2

Id Subject Object Predicate Lexical cue
T1 65-83 SpecificDisease denotes myotonic dystrophy
T2 326-344 SpecificDisease denotes myotonic dystrophy
T3 346-348 SpecificDisease denotes DM
T4 650-652 SpecificDisease denotes DM
T5 880-882 SpecificDisease denotes DM
T6 1166-1168 SpecificDisease denotes DM

NCBI-Disease-Test-4o-GuidelineInPrompt

Id Subject Object Predicate Lexical cue
T1 65-83 Modifier denotes myotonic dystrophy
T2 326-344 SpecificDisease denotes myotonic dystrophy
T3 650-652 SpecificDisease denotes DM
T4 880-882 Modifier denotes DM
T5 1166-1168 Modifier denotes DM

NCBI-Disease-Corpus-UpdatedGuideline

Id Subject Object Predicate Lexical cue
T1 65-83 SpecificDisease denotes myotonic dystrophy
T2 326-344 SpecificDisease denotes myotonic dystrophy
T3 650-652 SpecificDisease denotes DM
T4 657-685 DiseaseClass denotes other human genetic diseases
T5 880-882 SpecificDisease denotes DM
T6 1166-1168 SpecificDisease denotes DM

NCBI-Disease-Corpus-humanintheloop

Id Subject Object Predicate Lexical cue
T1 326-344 SpecificDisease denotes myotonic dystrophy
T2 346-348 SpecificDisease denotes DM
T3 650-652 SpecificDisease denotes DM
T4 880-882 SpecificDisease denotes DM
T5 1166-1168 SpecificDisease denotes DM
T6 1554-1558 Modifier denotes DMPK

NCBI-Disease-Corpus-rezarta1

Id Subject Object Predicate Lexical cue
T1 65-83 Modifier denotes myotonic dystrophy
T2 326-344 SpecificDisease denotes myotonic dystrophy
T3 650-652 SpecificDisease denotes DM
T4 880-882 Modifier denotes DM
T5 1166-1168 SpecificDisease denotes DM

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T117 65-83 Modifier denotes myotonic dystrophy D009223
T118 326-344 SpecificDisease denotes myotonic dystrophy D009223
T119 346-348 SpecificDisease denotes DM D009223
T120 650-652 SpecificDisease denotes DM D009223
T121 669-685 DiseaseClass denotes genetic diseases D030342
T122 880-882 Modifier denotes DM D009223
T123 1166-1168 Modifier denotes DM D009223

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 326-344 SpecificDisease denotes myotonic dystrophy
T2 346-348 SpecificDisease denotes DM
T3 650-652 SpecificDisease denotes DM
T4 880-882 SpecificDisease denotes DM
T5 1166-1168 SpecificDisease denotes DM

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 65-83 Modifier denotes myotonic dystrophy
T2 326-344 SpecificDisease denotes myotonic dystrophy
T3 650-652 SpecificDisease denotes DM
T4 880-882 Modifier denotes DM
T5 1166-1168 Modifier denotes DM

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 65-83 Modifier denotes myotonic dystrophy
T2 326-344 SpecificDisease denotes myotonic dystrophy
T3 650-652 Modifier denotes DM
T4 880-882 Modifier denotes DM
T5 1166-1168 Modifier denotes DM
T6 1554-1558 Modifier denotes DMPK

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 65-83 SpecificDisease denotes myotonic dystrophy
T2 326-349 SpecificDisease denotes myotonic dystrophy (DM)
T3 650-652 SpecificDisease denotes DM
T4 663-685 DiseaseClass denotes human genetic diseases
T5 874-882 SpecificDisease denotes human DM
T6 1166-1168 SpecificDisease denotes DM

123456

Id Subject Object Predicate Lexical cue
T1 326-344 SpecificDisease denotes myotonic dystrophy
T2 346-348 SpecificDisease denotes DM
T3 650-652 SpecificDisease denotes DM
T4 880-882 SpecificDisease denotes DM
T5 1166-1168 SpecificDisease denotes DM
T6 1554-1558 Modifier denotes DMPK

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Id Subject Object Predicate Lexical cue
T1 65-83 Modifier denotes myotonic dystrophy
T2 326-344 SpecificDisease denotes myotonic dystrophy
T3 346-348 SpecificDisease denotes DM
T4 650-652 SpecificDisease denotes DM
T5 880-882 Modifier denotes DM
T6 1166-1168 SpecificDisease denotes DM