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NCBI-Disease-Corpus-GPT5-withguidelines

Id Subject Object Predicate Lexical cue
T1 77-95 Modifier denotes myotonic dystrophy
T2 127-145 SpecificDisease denotes myotonic dystrophy
T3 147-149 SpecificDisease denotes DM
T4 215-217 Modifier denotes DM
T5 293-295 Modifier denotes DM
T6 963-965 Modifier denotes DM
T7 1053-1071 Modifier denotes myotonic dystrophy

NCBI-Disease-Corpus-GPT5-noguidelines

Id Subject Object Predicate Lexical cue
T1 77-95 SpecificDisease denotes myotonic dystrophy
T2 127-145 SpecificDisease denotes myotonic dystrophy
T3 147-149 SpecificDisease denotes DM
T4 293-295 SpecificDisease denotes DM
T5 644-651 DiseaseClass denotes disease
T6 963-965 SpecificDisease denotes DM
T7 1053-1071 SpecificDisease denotes myotonic dystrophy

NCBI-Disease-Corpus-GPT5-guidelineprompt

Id Subject Object Predicate Lexical cue
T1 77-95 Modifier denotes myotonic dystrophy
T2 127-145 SpecificDisease denotes myotonic dystrophy
T3 147-149 SpecificDisease denotes DM
T4 215-217 Modifier denotes DM
T5 293-295 Modifier denotes DM
T6 963-965 Modifier denotes DM
T7 1053-1071 Modifier denotes myotonic dystrophy

NCBI-Disease-Corpus-Moderated1

Id Subject Object Predicate Lexical cue
T1 77-95 Modifier denotes myotonic dystrophy
T2 147-149 SpecificDisease denotes DM
T3 215-217 Modifier denotes DM
T4 293-295 Modifier denotes DM
T5 963-965 Modifier denotes DM
T6 1053-1071 Modifier denotes myotonic dystrophy

DisGeNET

Id Subject Object Predicate Lexical cue
T0 204-207 gene:8170 denotes UTR
T1 127-145 disease:C0410226 denotes myotonic dystrophy
T2 204-207 gene:8170 denotes UTR
T3 127-145 disease:C0027126 denotes myotonic dystrophy
T4 204-207 gene:2837 denotes UTR
T5 127-145 disease:C0410226 denotes myotonic dystrophy
T6 204-207 gene:2837 denotes UTR
T7 127-145 disease:C0027126 denotes myotonic dystrophy
T8 204-207 gene:8170 denotes UTR
T9 147-149 disease:C0410226 denotes DM
T10 204-207 gene:8170 denotes UTR
T11 147-149 disease:C0027126 denotes DM
T12 204-207 gene:2837 denotes UTR
T13 147-149 disease:C0410226 denotes DM
T14 204-207 gene:2837 denotes UTR
T15 147-149 disease:C0027126 denotes DM
T16 215-232 gene:1760 denotes DM protein kinase
T17 127-145 disease:C0410226 denotes myotonic dystrophy
T18 215-232 gene:1760 denotes DM protein kinase
T19 127-145 disease:C0027126 denotes myotonic dystrophy
R1 T0 T1 associated_with UTR,myotonic dystrophy
R2 T2 T3 associated_with UTR,myotonic dystrophy
R3 T4 T5 associated_with UTR,myotonic dystrophy
R4 T6 T7 associated_with UTR,myotonic dystrophy
R5 T8 T9 associated_with UTR,DM
R6 T10 T11 associated_with UTR,DM
R7 T12 T13 associated_with UTR,DM
R8 T14 T15 associated_with UTR,DM
R9 T16 T17 associated_with DM protein kinase,myotonic dystrophy
R10 T18 T19 associated_with DM protein kinase,myotonic dystrophy

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
9425239-1#109#126#gene1760 215-232 gene1760 denotes DM protein kinase
9425239-1#21#39#diseaseC0027126 127-145 diseaseC0027126 denotes myotonic dystrophy
9425239-1#41#43#diseaseC0027126 147-149 diseaseC0027126 denotes DM
109#126#gene176021#39#diseaseC0027126 9425239-1#109#126#gene1760 9425239-1#21#39#diseaseC0027126 associated_with DM protein kinase,myotonic dystrophy
109#126#gene176041#43#diseaseC0027126 9425239-1#109#126#gene1760 9425239-1#41#43#diseaseC0027126 associated_with DM protein kinase,DM

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 77-95 Modifier:D009223 denotes myotonic dystrophy
T2 127-145 SpecificDisease:D009223 denotes myotonic dystrophy
T3 147-149 SpecificDisease:D009223 denotes DM
T4 215-217 Modifier:D009223 denotes DM
T5 293-295 Modifier:D009223 denotes DM
T6 963-965 Modifier:D009223 denotes DM
T7 1053-1071 Modifier:D009223 denotes myotonic dystrophy

NCBI-Disease-Test

Id Subject Object Predicate Lexical cue database_id
T714 77-95 Modifier denotes myotonic dystrophy D009223
T715 127-145 SpecificDisease denotes myotonic dystrophy D009223
T716 147-149 SpecificDisease denotes DM D009223
T717 215-217 Modifier denotes DM D009223
T718 293-295 Modifier denotes DM D009223
T719 963-965 Modifier denotes DM D009223
T720 1053-1071 Modifier denotes myotonic dystrophy D009223

NCBI-Disease-Test-Assistant-Knowledge

Id Subject Object Predicate Lexical cue
T1 77-95 SpecificDisease denotes myotonic dystrophy
T2 127-150 SpecificDisease denotes myotonic dystrophy (DM)
T3 644-651 SpecificDisease denotes disease
T4 1053-1071 SpecificDisease denotes myotonic dystrophy

NCBI-Disease-Test-4o-NoGuidelineInPrompt

Id Subject Object Predicate Lexical cue
T1 77-95 SpecificDisease denotes myotonic dystrophy
T2 127-150 SpecificDisease denotes myotonic dystrophy (DM)
T3 644-651 SpecificDisease denotes disease
T4 1053-1071 SpecificDisease denotes myotonic dystrophy

NCBI-Disease-Corpus-o3-2

Id Subject Object Predicate Lexical cue
T1 77-95 SpecificDisease denotes myotonic dystrophy
T2 127-145 SpecificDisease denotes myotonic dystrophy
T3 147-149 SpecificDisease denotes DM
T4 293-295 Modifier denotes DM
T5 963-965 Modifier denotes DM
T6 1053-1071 SpecificDisease denotes myotonic dystrophy

NCBI-Disease-Corpus-high-o3-1

Id Subject Object Predicate Lexical cue
T1 77-95 Modifier denotes myotonic dystrophy
T2 127-145 SpecificDisease denotes myotonic dystrophy
T3 147-149 SpecificDisease denotes DM
T4 293-295 Modifier denotes DM
T5 963-965 SpecificDisease denotes DM
T6 1053-1071 Modifier denotes myotonic dystrophy

NCBI-Disease-Corpus-high-o3-2

Id Subject Object Predicate Lexical cue
T1 77-95 Modifier denotes myotonic dystrophy
T2 127-145 SpecificDisease denotes myotonic dystrophy
T3 147-149 SpecificDisease denotes DM
T4 293-295 Modifier denotes DM
T5 963-965 Modifier denotes DM
T6 1053-1071 Modifier denotes myotonic dystrophy

NCBI-Disease-Test-4o-GuidelineInPrompt

Id Subject Object Predicate Lexical cue
T1 77-95 SpecificDisease denotes myotonic dystrophy
T2 127-145 SpecificDisease denotes myotonic dystrophy
T3 147-149 SpecificDisease denotes DM
T4 293-295 SpecificDisease denotes DM
T5 963-965 SpecificDisease denotes DM
T6 1053-1071 SpecificDisease denotes myotonic dystrophy

NCBI-Disease-Corpus-UpdatedGuideline

Id Subject Object Predicate Lexical cue
T1 77-95 SpecificDisease denotes myotonic dystrophy
T2 127-145 SpecificDisease denotes myotonic dystrophy
T3 147-149 SpecificDisease denotes DM
T4 293-295 SpecificDisease denotes DM
T5 963-965 SpecificDisease denotes DM
T6 1053-1071 SpecificDisease denotes myotonic dystrophy

NCBI-Disease-Corpus-humanintheloop

Id Subject Object Predicate Lexical cue
T1 77-95 Modifier denotes myotonic dystrophy
T2 127-145 SpecificDisease denotes myotonic dystrophy
T3 147-149 SpecificDisease denotes DM
T4 293-295 SpecificDisease denotes DM
T5 963-965 Modifier denotes DM
T6 1053-1071 Modifier denotes myotonic dystrophy

NCBI-Disease-Corpus-rezarta1

Id Subject Object Predicate Lexical cue
T1 77-95 SpecificDisease denotes myotonic dystrophy
T2 127-145 SpecificDisease denotes myotonic dystrophy
T3 147-149 SpecificDisease denotes DM
T4 215-217 Modifier denotes DM
T5 293-295 Modifier denotes DM
T6 963-965 Modifier denotes DM
T7 1053-1071 SpecificDisease denotes myotonic dystrophy

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T714 77-95 Modifier denotes myotonic dystrophy D009223
T715 127-145 SpecificDisease denotes myotonic dystrophy D009223
T716 147-149 SpecificDisease denotes DM D009223
T717 215-217 Modifier denotes DM D009223
T718 293-295 Modifier denotes DM D009223
T719 963-965 Modifier denotes DM D009223
T720 1053-1071 Modifier denotes myotonic dystrophy D009223

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 77-95 Modifier denotes myotonic dystrophy
T2 127-145 SpecificDisease denotes myotonic dystrophy
T3 147-149 SpecificDisease denotes DM
T4 293-295 SpecificDisease denotes DM
T5 963-965 Modifier denotes DM
T6 1053-1071 Modifier denotes myotonic dystrophy

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 77-95 Modifier denotes myotonic dystrophy
T2 127-145 SpecificDisease denotes myotonic dystrophy
T3 147-149 SpecificDisease denotes DM
T4 215-217 Modifier denotes DM
T5 293-295 Modifier denotes DM
T6 963-965 Modifier denotes DM
T7 1053-1071 Modifier denotes myotonic dystrophy

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 77-95 SpecificDisease denotes myotonic dystrophy
T2 127-145 SpecificDisease denotes myotonic dystrophy
T3 147-149 SpecificDisease denotes DM
T4 293-295 SpecificDisease denotes DM
T5 963-965 SpecificDisease denotes DM
T6 1053-1071 SpecificDisease denotes myotonic dystrophy

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 77-95 SpecificDisease denotes myotonic dystrophy
T2 127-150 SpecificDisease denotes myotonic dystrophy (DM)
T3 644-651 SpecificDisease denotes disease
T4 1053-1071 SpecificDisease denotes myotonic dystrophy

123456

Id Subject Object Predicate Lexical cue
T1 77-95 Modifier denotes myotonic dystrophy
T2 127-145 SpecificDisease denotes myotonic dystrophy
T3 147-149 SpecificDisease denotes DM
T4 293-295 SpecificDisease denotes DM
T5 963-965 Modifier denotes DM
T6 1053-1071 Modifier denotes myotonic dystrophy

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Id Subject Object Predicate Lexical cue
T1 77-95 SpecificDisease denotes myotonic dystrophy
T2 127-145 SpecificDisease denotes myotonic dystrophy
T3 147-149 SpecificDisease denotes DM
T4 215-217 Modifier denotes DM
T5 293-295 SpecificDisease denotes DM
T6 963-965 Modifier denotes DM
T7 1053-1071 SpecificDisease denotes myotonic dystrophy