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NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 40-82 SpecificDisease:D054067 denotes dihydropyrimidine dehydrogenase deficiency
T2 84-132 SpecificDisease:D054067 denotes Dihydropyrimidine dehydrogenase (DPD) deficiency
T3 139-166 DiseaseClass:D030342 denotes autosomal recessive disease
T4 356-370 SpecificDisease:D054067 denotes DPD deficiency
T5 438-455 SpecificDisease:D054067 denotes deficiency of DPD
T6 733-736 Modifier:D054067 denotes DPD
T7 971-991 DiseaseClass:D004829 denotes convulsive disorders
T8 993-1010 DiseaseClass:D019957 denotes motor retardation
T9 1015-1033 DiseaseClass:D008607 denotes mental retardation
T10 1238-1260 DiseaseClass:D013568 denotes clinical abnormalities
T11 1290-1304 SpecificDisease:D054067 denotes DPD deficiency

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 139-158 HP_0000007 denotes autosomal recessive
T2 192-202 HP_0012127 denotes uraciluria
T3 993-1010 HP_0001270 denotes motor retardation
T4 1015-1033 HP_0001249 denotes mental retardation

NCBI-Disease-Train

Id Subject Object Predicate Lexical cue database_id
T119 40-82 SpecificDisease denotes dihydropyrimidine dehydrogenase deficiency D054067
T120 84-132 SpecificDisease denotes Dihydropyrimidine dehydrogenase (DPD) deficiency D054067
T121 139-166 DiseaseClass denotes autosomal recessive disease D030342
T122 356-370 SpecificDisease denotes DPD deficiency D054067
T123 438-455 SpecificDisease denotes deficiency of DPD D054067
T124 733-736 Modifier denotes DPD D054067
T125 971-991 DiseaseClass denotes convulsive disorders D004829
T126 993-1010 DiseaseClass denotes motor retardation D019957
T127 1015-1033 DiseaseClass denotes mental retardation D008607
T128 1238-1260 DiseaseClass denotes clinical abnormalities D013568
T129 1290-1304 SpecificDisease denotes DPD deficiency D054067

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T119 40-82 SpecificDisease denotes dihydropyrimidine dehydrogenase deficiency D054067
T120 84-132 SpecificDisease denotes Dihydropyrimidine dehydrogenase (DPD) deficiency D054067
T121 139-166 DiseaseClass denotes autosomal recessive disease D030342
T122 356-370 SpecificDisease denotes DPD deficiency D054067
T123 438-455 SpecificDisease denotes deficiency of DPD D054067
T124 733-736 Modifier denotes DPD D054067
T125 971-991 DiseaseClass denotes convulsive disorders D004829
T126 993-1010 DiseaseClass denotes motor retardation D019957
T127 1015-1033 DiseaseClass denotes mental retardation D008607
T128 1238-1260 DiseaseClass denotes clinical abnormalities D013568
T129 1290-1304 SpecificDisease denotes DPD deficiency D054067

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 40-82 SpecificDisease denotes dihydropyrimidine dehydrogenase deficiency
T2 84-132 SpecificDisease denotes Dihydropyrimidine dehydrogenase (DPD) deficiency
T3 356-370 SpecificDisease denotes DPD deficiency
T4 452-455 SpecificDisease denotes DPD
T5 733-736 SpecificDisease denotes DPD
T6 971-991 DiseaseClass denotes convulsive disorders
T7 993-1010 DiseaseClass denotes motor retardation
T8 1015-1033 DiseaseClass denotes mental retardation
T9 1290-1304 SpecificDisease denotes DPD deficiency

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 40-82 SpecificDisease denotes dihydropyrimidine dehydrogenase deficiency
T4 184-202 DiseaseClass denotes thymine-uraciluria
T5 356-370 SpecificDisease denotes DPD deficiency
T6 452-455 Modifier denotes DPD
T7 733-736 Modifier denotes DPD
T8 971-991 DiseaseClass denotes convulsive disorders
T9 993-1010 DiseaseClass denotes motor retardation
T10 1015-1033 DiseaseClass denotes mental retardation
T11 1290-1304 SpecificDisease denotes DPD deficiency

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 40-82 SpecificDisease denotes dihydropyrimidine dehydrogenase deficiency
T2 84-132 SpecificDisease denotes Dihydropyrimidine dehydrogenase (DPD) deficiency
T3 139-166 DiseaseClass denotes autosomal recessive disease
T4 356-370 SpecificDisease denotes DPD deficiency
T5 452-455 SpecificDisease denotes DPD
T6 733-736 SpecificDisease denotes DPD
T7 971-991 DiseaseClass denotes convulsive disorders
T8 993-1010 DiseaseClass denotes motor retardation
T9 1015-1033 DiseaseClass denotes mental retardation
T10 1290-1304 SpecificDisease denotes DPD deficiency

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 40-82 SpecificDisease denotes dihydropyrimidine dehydrogenase deficiency
T2 84-132 SpecificDisease denotes Dihydropyrimidine dehydrogenase (DPD) deficiency
T3 159-166 DiseaseClass denotes disease
T4 356-370 SpecificDisease denotes DPD deficiency
T5 452-455 SpecificDisease denotes DPD
T6 733-745 SpecificDisease denotes DPD patients
T7 971-991 CompositeMention denotes convulsive disorders
T8 993-1010 CompositeMention denotes motor retardation
T9 1015-1033 CompositeMention denotes mental retardation
T10 1290-1304 SpecificDisease denotes DPD deficiency