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PubMed:9863607 JSONTXT

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NCBI-Disease-Corpus-GPT5-withguidelines

Id Subject Object Predicate Lexical cue
T1 26-44 SpecificDisease denotes myotonic dystrophy
T2 46-64 SpecificDisease denotes Myotonic dystrophy
T3 66-68 SpecificDisease denotes DM
T4 76-102 DiseaseClass denotes autosomal dominant disease
T5 198-209 DiseaseClass denotes infertility
T6 214-243 SpecificDisease denotes congenital myotonic dystrophy
T7 245-248 SpecificDisease denotes CDM
T8 276-278 SpecificDisease denotes DM
T9 405-407 Modifier denotes DM
T10 476-478 SpecificDisease denotes DM
T11 513-515 SpecificDisease denotes DM
T12 684-686 Modifier denotes DM
T13 915-917 SpecificDisease denotes DM
T14 980-982 Modifier denotes DM
T15 1069-1071 Modifier denotes DM

NCBI-Disease-Corpus-GPT5-noguidelines

Id Subject Object Predicate Lexical cue
T1 26-44 SpecificDisease denotes myotonic dystrophy
T2 46-69 CompositeMention denotes Myotonic dystrophy (DM)
T3 76-102 DiseaseClass denotes autosomal dominant disease
T4 198-209 SpecificDisease denotes infertility
T5 214-249 CompositeMention denotes congenital myotonic dystrophy (CDM)
T6 276-278 SpecificDisease denotes DM
T7 405-407 SpecificDisease denotes DM
T8 476-478 SpecificDisease denotes DM
T9 513-515 SpecificDisease denotes DM
T10 684-686 SpecificDisease denotes DM
T11 915-917 SpecificDisease denotes DM
T12 980-982 SpecificDisease denotes DM
T13 996-998 SpecificDisease denotes DM
T14 1069-1071 SpecificDisease denotes DM

NCBI-Disease-Corpus-GPT5-guidelineprompt

Id Subject Object Predicate Lexical cue
T1 26-44 SpecificDisease denotes myotonic dystrophy
T2 46-64 SpecificDisease denotes Myotonic dystrophy
T3 66-68 SpecificDisease denotes DM
T4 76-102 DiseaseClass denotes autosomal dominant disease
T5 198-209 DiseaseClass denotes infertility
T6 214-243 SpecificDisease denotes congenital myotonic dystrophy
T7 245-248 SpecificDisease denotes CDM
T8 276-278 SpecificDisease denotes DM
T9 405-407 Modifier denotes DM
T10 476-478 SpecificDisease denotes DM
T11 513-515 SpecificDisease denotes DM
T12 684-686 Modifier denotes DM
T13 915-917 SpecificDisease denotes DM
T14 980-982 Modifier denotes DM
T15 1069-1071 Modifier denotes DM

NCBI-Disease-Corpus-Moderated1

Id Subject Object Predicate Lexical cue
T1 26-44 SpecificDisease denotes myotonic dystrophy
T2 46-64 SpecificDisease denotes Myotonic dystrophy
T3 66-68 SpecificDisease denotes DM
T4 76-102 DiseaseClass denotes autosomal dominant disease
T5 214-243 SpecificDisease denotes congenital myotonic dystrophy
T6 245-248 SpecificDisease denotes CDM
T7 405-407 Modifier denotes DM
T8 476-478 SpecificDisease denotes DM
T9 684-686 Modifier denotes DM
T10 915-917 SpecificDisease denotes DM
T11 980-982 Modifier denotes DM
T12 992-998 Modifier denotes non-DM
T13 1069-1071 Modifier denotes DM

DisGeNET

Id Subject Object Predicate Lexical cue
T0 0-22 gene:5905 denotes Segregation distortion
T1 26-44 disease:C0027126 denotes myotonic dystrophy
T2 0-22 gene:5905 denotes Segregation distortion
T3 26-44 disease:C0410226 denotes myotonic dystrophy
R1 T0 T1 associated_with Segregation distortion,myotonic dystrophy
R2 T2 T3 associated_with Segregation distortion,myotonic dystrophy

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
9863607-0#0#22#gene5905 0-22 gene5905 denotes Segregation distortion
9863607-0#26#44#diseaseC0027126 26-44 diseaseC0027126 denotes myotonic dystrophy
0#22#gene590526#44#diseaseC0027126 9863607-0#0#22#gene5905 9863607-0#26#44#diseaseC0027126 associated_with Segregation distortion,myotonic dystrophy

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 26-44 SpecificDisease:D009223 denotes myotonic dystrophy
T2 46-64 SpecificDisease:D009223 denotes Myotonic dystrophy
T3 66-68 SpecificDisease:D009223 denotes DM
T4 76-102 DiseaseClass:D030342 denotes autosomal dominant disease
T5 198-209 SpecificDisease:D007246 denotes infertility
T6 214-243 SpecificDisease:D009223 denotes congenital myotonic dystrophy
T7 245-248 SpecificDisease:D009223 denotes CDM
T8 276-278 SpecificDisease:D009223 denotes DM
T9 405-407 Modifier:D009223 denotes DM
T10 476-478 SpecificDisease:D009223 denotes DM
T11 513-515 SpecificDisease:D009223 denotes DM
T12 684-686 Modifier:D009223 denotes DM
T13 915-917 SpecificDisease:D009223 denotes DM
T14 980-982 Modifier:D009223 denotes DM
T15 1069-1071 Modifier:D009223 denotes DM

NCBI-Disease-Test

Id Subject Object Predicate Lexical cue database_id
T69 26-44 SpecificDisease denotes myotonic dystrophy D009223
T70 46-64 SpecificDisease denotes Myotonic dystrophy D009223
T71 66-68 SpecificDisease denotes DM D009223
T72 76-102 DiseaseClass denotes autosomal dominant disease D030342
T73 198-209 SpecificDisease denotes infertility D007246
T74 214-243 SpecificDisease denotes congenital myotonic dystrophy D009223
T75 245-248 SpecificDisease denotes CDM D009223
T76 276-278 SpecificDisease denotes DM D009223
T77 405-407 Modifier denotes DM D009223
T78 476-478 SpecificDisease denotes DM D009223
T79 513-515 SpecificDisease denotes DM D009223
T80 684-686 Modifier denotes DM D009223
T81 915-917 SpecificDisease denotes DM D009223
T82 980-982 Modifier denotes DM D009223
T83 1069-1071 Modifier denotes DM D009223

NCBI-Disease-Test-Assistant-Knowledge

Id Subject Object Predicate Lexical cue
T1 26-44 SpecificDisease denotes myotonic dystrophy
T2 46-69 SpecificDisease denotes Myotonic dystrophy (DM)
T3 214-249 SpecificDisease denotes congenital myotonic dystrophy (CDM)
T4 276-278 SpecificDisease denotes DM
T5 405-407 SpecificDisease denotes DM
T6 476-478 SpecificDisease denotes DM
T7 513-515 SpecificDisease denotes DM
T8 684-686 SpecificDisease denotes DM
T9 915-917 SpecificDisease denotes DM
T10 980-982 SpecificDisease denotes DM
T11 996-998 SpecificDisease denotes DM
T12 1069-1071 SpecificDisease denotes DM

NCBI-Disease-Test-4o-NoGuidelineInPrompt

Id Subject Object Predicate Lexical cue
T1 26-44 SpecificDisease denotes myotonic dystrophy
T2 46-69 SpecificDisease denotes Myotonic dystrophy (DM)
T3 214-249 SpecificDisease denotes congenital myotonic dystrophy (CDM)
T4 276-278 SpecificDisease denotes DM
T5 405-407 SpecificDisease denotes DM
T6 476-478 SpecificDisease denotes DM
T7 513-515 SpecificDisease denotes DM
T8 684-686 SpecificDisease denotes DM
T9 915-917 SpecificDisease denotes DM
T10 980-982 SpecificDisease denotes DM
T11 996-998 SpecificDisease denotes DM
T12 1069-1071 SpecificDisease denotes DM

NCBI-Disease-Corpus-o3-2

Id Subject Object Predicate Lexical cue
T1 26-44 SpecificDisease denotes myotonic dystrophy
T2 46-64 SpecificDisease denotes Myotonic dystrophy
T3 66-68 SpecificDisease denotes DM
T4 214-243 SpecificDisease denotes congenital myotonic dystrophy
T5 245-248 SpecificDisease denotes CDM
T6 276-278 SpecificDisease denotes DM
T7 405-407 SpecificDisease denotes DM
T8 476-478 SpecificDisease denotes DM
T9 513-515 SpecificDisease denotes DM
T10 684-686 SpecificDisease denotes DM
T11 915-917 SpecificDisease denotes DM
T12 980-982 SpecificDisease denotes DM
T13 996-998 SpecificDisease denotes DM
T14 1069-1071 SpecificDisease denotes DM

NCBI-Disease-Corpus-high-o3-1

Id Subject Object Predicate Lexical cue
T1 26-44 SpecificDisease denotes myotonic dystrophy
T2 46-64 SpecificDisease denotes Myotonic dystrophy
T3 66-68 SpecificDisease denotes DM
T4 214-243 SpecificDisease denotes congenital myotonic dystrophy
T5 245-248 SpecificDisease denotes CDM
T6 276-278 SpecificDisease denotes DM
T7 405-407 SpecificDisease denotes DM
T8 476-478 SpecificDisease denotes DM
T9 513-515 SpecificDisease denotes DM
T10 684-686 SpecificDisease denotes DM
T11 915-917 SpecificDisease denotes DM
T12 980-982 SpecificDisease denotes DM
T13 996-998 Modifier denotes DM
T14 1069-1071 SpecificDisease denotes DM

NCBI-Disease-Corpus-high-o3-2

Id Subject Object Predicate Lexical cue
T1 26-44 SpecificDisease denotes myotonic dystrophy
T2 46-64 SpecificDisease denotes Myotonic dystrophy
T3 66-68 SpecificDisease denotes DM
T4 214-243 SpecificDisease denotes congenital myotonic dystrophy
T5 245-248 SpecificDisease denotes CDM
T6 276-278 SpecificDisease denotes DM
T7 405-407 SpecificDisease denotes DM
T8 476-478 SpecificDisease denotes DM
T9 513-515 SpecificDisease denotes DM
T10 684-686 SpecificDisease denotes DM
T11 915-917 SpecificDisease denotes DM
T12 980-982 SpecificDisease denotes DM
T13 1069-1071 SpecificDisease denotes DM

NCBI-Disease-Test-4o-GuidelineInPrompt

Id Subject Object Predicate Lexical cue
T1 26-44 SpecificDisease denotes myotonic dystrophy
T2 46-64 SpecificDisease denotes Myotonic dystrophy
T3 66-68 SpecificDisease denotes DM
T4 76-102 DiseaseClass denotes autosomal dominant disease
T5 214-243 SpecificDisease denotes congenital myotonic dystrophy
T6 245-248 SpecificDisease denotes CDM
T7 276-278 SpecificDisease denotes DM
T8 405-407 SpecificDisease denotes DM
T9 476-478 SpecificDisease denotes DM
T10 513-515 SpecificDisease denotes DM
T11 684-686 SpecificDisease denotes DM
T12 915-917 SpecificDisease denotes DM
T13 980-982 SpecificDisease denotes DM
T14 996-998 SpecificDisease denotes DM
T15 1069-1071 SpecificDisease denotes DM

NCBI-Disease-Corpus-UpdatedGuideline

Id Subject Object Predicate Lexical cue
T1 26-44 SpecificDisease denotes myotonic dystrophy
T2 46-64 SpecificDisease denotes Myotonic dystrophy
T3 66-68 SpecificDisease denotes DM
T4 76-102 DiseaseClass denotes autosomal dominant disease
T5 214-243 SpecificDisease denotes congenital myotonic dystrophy
T6 245-248 SpecificDisease denotes CDM
T7 276-278 SpecificDisease denotes DM
T8 405-407 SpecificDisease denotes DM
T9 476-478 SpecificDisease denotes DM
T10 513-515 SpecificDisease denotes DM
T11 684-686 SpecificDisease denotes DM
T12 915-917 SpecificDisease denotes DM
T13 980-982 SpecificDisease denotes DM
T14 996-998 SpecificDisease denotes DM
T15 1069-1071 SpecificDisease denotes DM

NCBI-Disease-Corpus-humanintheloop

Id Subject Object Predicate Lexical cue
T1 26-44 SpecificDisease denotes myotonic dystrophy
T2 46-64 SpecificDisease denotes Myotonic dystrophy
T3 66-68 SpecificDisease denotes DM
T4 214-243 SpecificDisease denotes congenital myotonic dystrophy
T5 245-248 SpecificDisease denotes CDM
T6 276-278 SpecificDisease denotes DM
T7 405-407 Modifier denotes DM
T8 476-478 SpecificDisease denotes DM
T9 513-515 SpecificDisease denotes DM
T10 684-686 Modifier denotes DM
T11 915-917 SpecificDisease denotes DM
T12 980-982 Modifier denotes DM
T13 996-998 Modifier denotes DM
T14 1069-1071 Modifier denotes DM

NCBI-Disease-Corpus-rezarta1

Id Subject Object Predicate Lexical cue
T1 26-44 SpecificDisease denotes myotonic dystrophy
T2 46-64 SpecificDisease denotes Myotonic dystrophy
T3 66-68 SpecificDisease denotes DM
T4 214-243 SpecificDisease denotes congenital myotonic dystrophy
T5 245-248 SpecificDisease denotes CDM
T6 276-278 Modifier denotes DM
T7 405-407 Modifier denotes DM
T8 476-478 SpecificDisease denotes DM
T9 513-515 SpecificDisease denotes DM
T10 684-686 Modifier denotes DM
T11 915-917 SpecificDisease denotes DM
T12 980-982 Modifier denotes DM
T13 1069-1071 Modifier denotes DM

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T69 26-44 SpecificDisease denotes myotonic dystrophy D009223
T70 46-64 SpecificDisease denotes Myotonic dystrophy D009223
T71 66-68 SpecificDisease denotes DM D009223
T72 76-102 DiseaseClass denotes autosomal dominant disease D030342
T73 198-209 SpecificDisease denotes infertility D007246
T74 214-243 SpecificDisease denotes congenital myotonic dystrophy D009223
T75 245-248 SpecificDisease denotes CDM D009223
T76 276-278 SpecificDisease denotes DM D009223
T77 405-407 Modifier denotes DM D009223
T78 476-478 SpecificDisease denotes DM D009223
T79 513-515 SpecificDisease denotes DM D009223
T80 684-686 Modifier denotes DM D009223
T81 915-917 SpecificDisease denotes DM D009223
T82 980-982 Modifier denotes DM D009223
T83 1069-1071 Modifier denotes DM D009223

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 26-44 SpecificDisease denotes myotonic dystrophy
T2 46-64 SpecificDisease denotes Myotonic dystrophy
T3 66-68 SpecificDisease denotes DM
T4 214-243 SpecificDisease denotes congenital myotonic dystrophy
T5 245-248 SpecificDisease denotes CDM
T6 276-278 SpecificDisease denotes DM
T7 405-407 Modifier denotes DM
T8 476-478 SpecificDisease denotes DM
T9 513-515 SpecificDisease denotes DM
T10 684-686 Modifier denotes DM
T11 915-917 SpecificDisease denotes DM
T12 980-982 Modifier denotes DM
T13 996-998 Modifier denotes DM
T14 1069-1071 Modifier denotes DM

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 26-44 SpecificDisease denotes myotonic dystrophy
T2 46-64 SpecificDisease denotes Myotonic dystrophy
T3 66-68 SpecificDisease denotes DM
T4 225-243 SpecificDisease denotes myotonic dystrophy
T5 245-248 SpecificDisease denotes CDM
T6 276-278 SpecificDisease denotes DM
T7 405-407 Modifier denotes DM
T8 476-478 SpecificDisease denotes DM
T9 513-515 SpecificDisease denotes DM
T10 684-686 SpecificDisease denotes DM
T11 915-917 SpecificDisease denotes DM
T12 980-982 Modifier denotes DM
T13 1069-1071 SpecificDisease denotes DM

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 26-44 SpecificDisease denotes myotonic dystrophy
T2 46-64 SpecificDisease denotes Myotonic dystrophy
T3 66-68 SpecificDisease denotes DM
T4 76-102 DiseaseClass denotes autosomal dominant disease
T5 214-243 SpecificDisease denotes congenital myotonic dystrophy
T6 245-248 SpecificDisease denotes CDM
T7 276-278 SpecificDisease denotes DM
T8 405-407 SpecificDisease denotes DM
T9 476-478 SpecificDisease denotes DM
T10 513-515 SpecificDisease denotes DM
T11 684-686 SpecificDisease denotes DM
T12 915-917 SpecificDisease denotes DM
T13 980-982 SpecificDisease denotes DM
T14 996-998 SpecificDisease denotes DM
T15 1069-1071 SpecificDisease denotes DM

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 26-44 SpecificDisease denotes myotonic dystrophy
T2 46-69 SpecificDisease denotes Myotonic dystrophy (DM)
T3 214-249 SpecificDisease denotes congenital myotonic dystrophy (CDM)
T4 276-278 SpecificDisease denotes DM
T5 405-407 SpecificDisease denotes DM
T6 476-478 SpecificDisease denotes DM
T7 513-515 SpecificDisease denotes DM
T8 684-686 SpecificDisease denotes DM
T9 915-917 SpecificDisease denotes DM
T10 980-982 SpecificDisease denotes DM
T11 996-998 SpecificDisease denotes DM
T12 1069-1071 SpecificDisease denotes DM

123456

Id Subject Object Predicate Lexical cue
T1 26-44 SpecificDisease denotes myotonic dystrophy
T2 46-64 SpecificDisease denotes Myotonic dystrophy
T3 66-68 SpecificDisease denotes DM
T4 214-243 SpecificDisease denotes congenital myotonic dystrophy
T5 245-248 SpecificDisease denotes CDM
T6 276-278 SpecificDisease denotes DM
T7 405-407 Modifier denotes DM
T8 476-478 SpecificDisease denotes DM
T9 513-515 SpecificDisease denotes DM
T10 684-686 Modifier denotes DM
T11 915-917 SpecificDisease denotes DM
T12 980-982 Modifier denotes DM
T13 996-998 Modifier denotes DM
T14 1069-1071 Modifier denotes DM

12345

Id Subject Object Predicate Lexical cue
T1 26-44 SpecificDisease denotes myotonic dystrophy
T2 46-64 SpecificDisease denotes Myotonic dystrophy
T3 66-68 SpecificDisease denotes DM
T4 214-243 SpecificDisease denotes congenital myotonic dystrophy
T5 245-248 SpecificDisease denotes CDM
T6 276-278 SpecificDisease denotes DM
T7 405-407 Modifier denotes DM
T8 476-478 SpecificDisease denotes DM
T9 513-515 SpecificDisease denotes DM
T10 684-686 SpecificDisease denotes DM
T11 915-917 SpecificDisease denotes DM
T12 980-982 Modifier denotes DM
T13 996-998 SpecificDisease denotes DM
T14 1069-1071 SpecificDisease denotes DM