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PubMed:9020847 JSONTXT

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DisGeNET

Id Subject Object Predicate Lexical cue
T0 223-240 gene:1760 denotes DM protein kinase
T1 90-108 disease:C0410226 denotes Myotonic dystrophy
T2 223-240 gene:1760 denotes DM protein kinase
T3 90-108 disease:C0027126 denotes Myotonic dystrophy
T4 223-240 gene:1760 denotes DM protein kinase
T5 110-112 disease:C0410226 denotes DM
T6 223-240 gene:1760 denotes DM protein kinase
T7 110-112 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

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
9020847-1#133#150#gene1760 223-240 gene1760 denotes DM protein kinase
9020847-1#0#18#diseaseC0027126 90-108 diseaseC0027126 denotes Myotonic dystrophy
9020847-1#20#22#diseaseC0027126 110-112 diseaseC0027126 denotes DM
133#150#gene17600#18#diseaseC0027126 9020847-1#133#150#gene1760 9020847-1#0#18#diseaseC0027126 associated_with DM protein kinase,Myotonic dystrophy
133#150#gene176020#22#diseaseC0027126 9020847-1#133#150#gene1760 9020847-1#20#22#diseaseC0027126 associated_with DM protein kinase,DM

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 90-108 SpecificDisease:D009223 denotes Myotonic dystrophy
T2 110-112 SpecificDisease:D009223 denotes DM
T3 223-225 Modifier:D009223 denotes DM
T4 725-727 Modifier:D009223 denotes DM

ncbi-valid-gpt-nr-g

Id Subject Object Predicate Lexical cue
T1 90-108 SpecificDisease denotes Myotonic dystrophy
T2 110-112 SpecificDisease denotes DM
T3 725-727 Modifier denotes DM

ncbi-valid

Id Subject Object Predicate Lexical cue
T1 90-108 SpecificDisease denotes Myotonic dystrophy
T2 110-112 SpecificDisease denotes DM
T3 223-225 Modifier denotes DM
T4 725-727 Modifier denotes DM

ncbi-valid-gpt-r-ng

Id Subject Object Predicate Lexical cue
T1 90-108 SpecificDisease denotes Myotonic dystrophy
T2 110-112 SpecificDisease denotes DM
T3 223-225 SpecificDisease denotes DM
T4 334-344 Modifier denotes unaffected
T5 517-534 Modifier denotes clinical severity
T6 539-551 Modifier denotes age of onset
T7 725-727 SpecificDisease denotes DM
T8 1015-1030 Modifier denotes mildly affected

ncbi-valid-gpt-r-g

Id Subject Object Predicate Lexical cue
T1 90-108 SpecificDisease denotes Myotonic dystrophy
T2 110-112 SpecificDisease denotes DM
T3 223-225 Modifier denotes DM
T4 725-727 Modifier denotes DM

ncbi-valid-gpt-nr-ng

Id Subject Object Predicate Lexical cue
T1 90-113 SpecificDisease denotes Myotonic dystrophy (DM)

ncbi-valid-gemini-nr-ng

Id Subject Object Predicate Lexical cue
T1 90-108 SpecificDisease denotes Myotonic dystrophy
T2 110-112 SpecificDisease denotes DM
T3 247-249 SpecificDisease denotes DM
T4 1015-1038 CompositeMention denotes mildly affected patient

ncbi-valid-gemini-nr-g

Id Subject Object Predicate Lexical cue
T1 90-108 SpecificDisease denotes Myotonic dystrophy
T2 110-112 SpecificDisease denotes DM

ncbi-valid-gemini-r-g

Id Subject Object Predicate Lexical cue
T1 90-108 SpecificDisease denotes Myotonic dystrophy
T2 110-112 SpecificDisease denotes DM
T3 223-225 Modifier denotes DM
T4 725-727 Modifier denotes DM

ncbi-valid-deepseek-nr-ng

Id Subject Object Predicate Lexical cue
T1 0-8 Modifier denotes Moderate
T2 9-26 Modifier denotes intergenerational
T3 31-38 Modifier denotes somatic
T4 39-50 Modifier denotes instability
T5 56-69 CompositeMention denotes 55-CTG repeat
T6 73-88 CompositeMention denotes transgenic mice
T7 90-108 SpecificDisease denotes Myotonic dystrophy
T8 110-112 SpecificDisease denotes DM
T9 153-156 CompositeMention denotes CTG
T10 159-179 CompositeMention denotes trinucleotide repeat
T11 211-214 CompositeMention denotes UTR
T12 247-251 CompositeMention denotes DMPK
T13 259-262 CompositeMention denotes CTG
T14 377-384 CompositeMention denotes patient
T15 557-568 Modifier denotes instability
T16 685-696 Modifier denotes instability
T17 728-735 CompositeMention denotes tissues
T18 749-758 Modifier denotes mosaicism
T19 883-890 Modifier denotes genomic
T20 940-944 CompositeMention denotes mice
T21 972-979 CompositeMention denotes segment
T22 987-1000 CompositeMention denotes 55-CTG repeat
T23 1061-1073 CompositeMention denotes mouse models
T24 1085-1088 CompositeMention denotes CAG
T25 1104-1109 CompositeMention denotes cDNAs
T26 1134-1151 Modifier denotes intergenerational
T27 1156-1163 Modifier denotes somatic

ncbi-valid-deepseek-nr-g

Id Subject Object Predicate Lexical cue
T1 90-108 SpecificDisease denotes Myotonic dystrophy
T2 110-112 SpecificDisease denotes DM

ncbi-valid-deepseek-r-ng

Id Subject Object Predicate Lexical cue
T1 90-108 SpecificDisease denotes Myotonic dystrophy
T2 110-112 SpecificDisease denotes DM
T3 517-534 Modifier denotes clinical severity
T4 539-551 Modifier denotes age of onset

ncbi-valid-deepseek-r-g

Id Subject Object Predicate Lexical cue
T1 90-108 SpecificDisease denotes Myotonic dystrophy
T2 110-112 SpecificDisease denotes DM
T3 223-225 Modifier denotes DM

ncbi-valid-gemini-r-ng

Id Subject Object Predicate Lexical cue
T1 90-108 SpecificDisease denotes Myotonic dystrophy
T2 110-112 SpecificDisease denotes DM
T3 247-249 SpecificDisease denotes DM
T4 336-344 Modifier denotes affected
T5 1015-1030 Modifier denotes mildly affected

ncbi-valid-gemini-r-m

Id Subject Object Predicate Lexical cue
T1 90-108 SpecificDisease denotes Myotonic dystrophy
T2 110-112 SpecificDisease denotes DM
T3 223-225 Modifier denotes DM
T4 725-727 Modifier denotes DM

ncbi-valid-gpt-r-m

Id Subject Object Predicate Lexical cue
T1 90-108 SpecificDisease denotes Myotonic dystrophy
T2 110-112 SpecificDisease denotes DM
T3 223-225 Modifier denotes DM
T4 725-727 Modifier denotes DM

ncbi-valid-deepseek-r-m

Id Subject Object Predicate Lexical cue
T1 90-108 SpecificDisease denotes Myotonic dystrophy
T2 110-112 SpecificDisease denotes DM
T3 247-249 Modifier denotes DM

NCBI-Disease-Develop

Id Subject Object Predicate Lexical cue database_id
T142 90-108 SpecificDisease denotes Myotonic dystrophy D009223
T143 110-112 SpecificDisease denotes DM D009223
T144 223-225 Modifier denotes DM D009223
T145 725-727 Modifier denotes DM D009223

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T142 90-108 SpecificDisease denotes Myotonic dystrophy D009223
T143 110-112 SpecificDisease denotes DM D009223
T144 223-225 Modifier denotes DM D009223
T145 725-727 Modifier denotes DM D009223

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 90-108 SpecificDisease denotes Myotonic dystrophy
T2 110-112 SpecificDisease denotes DM
T3 223-225 Modifier denotes DM
T4 725-727 Modifier denotes DM

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 90-108 SpecificDisease denotes Myotonic dystrophy
T2 110-112 SpecificDisease denotes DM
T3 725-727 SpecificDisease denotes DM

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 90-108 SpecificDisease denotes Myotonic dystrophy
T2 110-112 SpecificDisease denotes DM
T3 725-727 SpecificDisease denotes DM

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 90-113 SpecificDisease denotes Myotonic dystrophy (DM)
T2 1015-1030 Modifier denotes mildly affected