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PubMed:10699184 JSONTXT

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FSU-PRGE

Id Subject Object Predicate Lexical cue
T1 63-96 protein denotes myotonic dystrophy protein kinase
T2 98-102 protein denotes DMPK
T3 318-351 protein denotes myotonic dystrophy protein kinase
T4 354-358 protein denotes DMPK
T5 410-414 protein denotes DMPK
T6 488-492 protein denotes DMPK
T7 512-516 protein denotes DMPK
T8 1543-1547 protein denotes DMPK

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
10699184-7#15#19#gene1760 1543-1547 gene1760 denotes DMPK
10699184-7#141#143#diseaseC0027126 1669-1671 diseaseC0027126 denotes DM
15#19#gene1760141#143#diseaseC0027126 10699184-7#15#19#gene1760 10699184-7#141#143#diseaseC0027126 associated_with DMPK,DM

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 63-81 Modifier:D009223 denotes myotonic dystrophy
T2 139-157 SpecificDisease:D009223 denotes Myotonic dystrophy
T3 159-161 SpecificDisease:D009223 denotes DM
T4 185-216 DiseaseClass:D009468+D030342 denotes inherited neuromuscular disease
T5 232-246 DiseaseClass:D030342 denotes genetic defect
T6 318-336 Modifier:D009223 denotes myotonic dystrophy
T7 1669-1671 Modifier:D009223 denotes DM

DisGeNET

Id Subject Object Predicate Lexical cue
T0 1543-1547 gene:1760 denotes DMPK
T1 1669-1671 disease:C0410226 denotes DM
T2 1543-1547 gene:1760 denotes DMPK
T3 1669-1671 disease:C0027126 denotes DM
R1 T0 T1 associated_with DMPK,DM
R2 T2 T3 associated_with DMPK,DM

NCBI-Disease-Train

Id Subject Object Predicate Lexical cue database_id
T646 63-81 Modifier denotes myotonic dystrophy D009223
T647 139-157 SpecificDisease denotes Myotonic dystrophy D009223
T648 159-161 SpecificDisease denotes DM D009223
T649 185-216 DiseaseClass denotes inherited neuromuscular disease D009468+D030342
T650 232-246 DiseaseClass denotes genetic defect D030342
T651 318-336 Modifier denotes myotonic dystrophy D009223
T652 1669-1671 Modifier denotes DM D009223

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T646 63-81 Modifier denotes myotonic dystrophy D009223
T647 139-157 SpecificDisease denotes Myotonic dystrophy D009223
T648 159-161 SpecificDisease denotes DM D009223
T649 185-216 DiseaseClass denotes inherited neuromuscular disease D009468+D030342
T650 232-246 DiseaseClass denotes genetic defect D030342
T651 318-336 Modifier denotes myotonic dystrophy D009223
T652 1669-1671 Modifier denotes DM D009223

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 63-81 Modifier denotes myotonic dystrophy
T2 139-157 SpecificDisease denotes Myotonic dystrophy
T3 159-161 SpecificDisease denotes DM
T4 318-336 Modifier denotes myotonic dystrophy
T5 1669-1671 SpecificDisease denotes DM

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 63-81 Modifier denotes myotonic dystrophy
T2 139-157 SpecificDisease denotes Myotonic dystrophy
T3 318-336 Modifier denotes myotonic dystrophy
T4 1669-1671 Modifier denotes DM

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 63-81 SpecificDisease denotes myotonic dystrophy
T2 139-162 SpecificDisease denotes Myotonic dystrophy (DM)
T3 195-216 Modifier denotes neuromuscular disease
T4 318-336 SpecificDisease denotes myotonic dystrophy

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 63-81 SpecificDisease denotes myotonic dystrophy
T2 139-162 SpecificDisease denotes Myotonic dystrophy (DM)
T3 209-216 DiseaseClass denotes disease
T4 318-336 SpecificDisease denotes myotonic dystrophy
T5 1669-1671 SpecificDisease denotes DM