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NCBI-Disease-Corpus-GPT5-withguidelines

Id Subject Object Predicate Lexical cue
T1 65-90 Modifier denotes hereditary coproporphyria
T2 99-124 SpecificDisease denotes Hereditary coproporphyria
T3 126-129 SpecificDisease denotes HCP
T4 137-163 DiseaseClass denotes autosomal dominant disease
T5 183-223 SpecificDisease denotes deficiency of coproporphyrinogen oxidase
T6 320-323 Modifier denotes HCP

NCBI-Disease-Corpus-GPT5-noguidelines

Id Subject Object Predicate Lexical cue
T1 65-90 SpecificDisease denotes hereditary coproporphyria
T2 99-124 SpecificDisease denotes Hereditary coproporphyria
T3 126-129 SpecificDisease denotes HCP
T4 137-155 Modifier denotes autosomal dominant
T5 183-223 SpecificDisease denotes deficiency of coproporphyrinogen oxidase
T6 320-323 SpecificDisease denotes HCP

NCBI-Disease-Corpus-GPT5-guidelineprompt

Id Subject Object Predicate Lexical cue
T1 65-90 Modifier denotes hereditary coproporphyria
T2 99-124 SpecificDisease denotes Hereditary coproporphyria
T3 126-129 SpecificDisease denotes HCP
T4 137-163 DiseaseClass denotes autosomal dominant disease
T5 183-223 SpecificDisease denotes deficiency of coproporphyrinogen oxidase
T6 320-323 Modifier denotes HCP

NCBI-Disease-Corpus-Moderated1

Id Subject Object Predicate Lexical cue
T1 65-90 Modifier denotes hereditary coproporphyria
T2 99-124 SpecificDisease denotes Hereditary coproporphyria
T3 126-129 SpecificDisease denotes HCP
T4 137-163 DiseaseClass denotes autosomal dominant disease
T5 183-223 SpecificDisease denotes deficiency of coproporphyrinogen oxidase
T6 320-323 Modifier denotes HCP

DisGeNET

Id Subject Object Predicate Lexical cue
T0 197-223 gene:1371 denotes coproporphyrinogen oxidase
T1 99-124 disease:C0162531 denotes Hereditary coproporphyria
T2 197-223 gene:1371 denotes coproporphyrinogen oxidase
T3 126-129 disease:C0162531 denotes HCP
T4 225-228 gene:1371 denotes CPO
T5 99-124 disease:C0162531 denotes Hereditary coproporphyria
T6 225-228 gene:1371 denotes CPO
T7 126-129 disease:C0162531 denotes HCP
T8 258-261 gene:1371 denotes CPO
T9 99-124 disease:C0162531 denotes Hereditary coproporphyria
T10 258-261 gene:1371 denotes CPO
T11 126-129 disease:C0162531 denotes HCP
R1 T0 T1 associated_with coproporphyrinogen oxidase,Hereditary coproporphyria
R2 T2 T3 associated_with coproporphyrinogen oxidase,HCP
R3 T4 T5 associated_with CPO,Hereditary coproporphyria
R4 T6 T7 associated_with CPO,HCP
R5 T8 T9 associated_with CPO,Hereditary coproporphyria
R6 T10 T11 associated_with CPO,HCP

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
9843038-1#98#124#gene1371 197-223 gene1371 denotes coproporphyrinogen oxidase
9843038-1#126#129#gene1371 225-228 gene1371 denotes CPO
9843038-1#159#162#gene1371 258-261 gene1371 denotes CPO
9843038-1#0#25#diseaseC0162531 99-124 diseaseC0162531 denotes Hereditary coproporphyria
9843038-1#27#30#diseaseC0162531 126-129 diseaseC0162531 denotes HCP
9843038-1#0#25#diseaseC0162531 99-124 diseaseC0162531 denotes Hereditary coproporphyria
9843038-1#27#30#diseaseC0162531 126-129 diseaseC0162531 denotes HCP
9843038-1#0#25#diseaseC0162531 99-124 diseaseC0162531 denotes Hereditary coproporphyria
98#124#gene13710#25#diseaseC0162531 9843038-1#98#124#gene1371 9843038-1#0#25#diseaseC0162531 associated_with coproporphyrinogen oxidase,Hereditary coproporphyria
98#124#gene137127#30#diseaseC0162531 9843038-1#98#124#gene1371 9843038-1#27#30#diseaseC0162531 associated_with coproporphyrinogen oxidase,HCP
98#124#gene13710#25#diseaseC0162531 9843038-1#98#124#gene1371 9843038-1#0#25#diseaseC0162531 associated_with coproporphyrinogen oxidase,Hereditary coproporphyria
98#124#gene137127#30#diseaseC0162531 9843038-1#98#124#gene1371 9843038-1#27#30#diseaseC0162531 associated_with coproporphyrinogen oxidase,HCP
98#124#gene13710#25#diseaseC0162531 9843038-1#98#124#gene1371 9843038-1#0#25#diseaseC0162531 associated_with coproporphyrinogen oxidase,Hereditary coproporphyria
126#129#gene13710#25#diseaseC0162531 9843038-1#126#129#gene1371 9843038-1#0#25#diseaseC0162531 associated_with CPO,Hereditary coproporphyria
126#129#gene137127#30#diseaseC0162531 9843038-1#126#129#gene1371 9843038-1#27#30#diseaseC0162531 associated_with CPO,HCP
126#129#gene13710#25#diseaseC0162531 9843038-1#126#129#gene1371 9843038-1#0#25#diseaseC0162531 associated_with CPO,Hereditary coproporphyria
126#129#gene137127#30#diseaseC0162531 9843038-1#126#129#gene1371 9843038-1#27#30#diseaseC0162531 associated_with CPO,HCP
126#129#gene13710#25#diseaseC0162531 9843038-1#126#129#gene1371 9843038-1#0#25#diseaseC0162531 associated_with CPO,Hereditary coproporphyria
159#162#gene13710#25#diseaseC0162531 9843038-1#159#162#gene1371 9843038-1#0#25#diseaseC0162531 associated_with CPO,Hereditary coproporphyria
159#162#gene137127#30#diseaseC0162531 9843038-1#159#162#gene1371 9843038-1#27#30#diseaseC0162531 associated_with CPO,HCP
159#162#gene13710#25#diseaseC0162531 9843038-1#159#162#gene1371 9843038-1#0#25#diseaseC0162531 associated_with CPO,Hereditary coproporphyria
159#162#gene137127#30#diseaseC0162531 9843038-1#159#162#gene1371 9843038-1#27#30#diseaseC0162531 associated_with CPO,HCP
159#162#gene13710#25#diseaseC0162531 9843038-1#159#162#gene1371 9843038-1#0#25#diseaseC0162531 associated_with CPO,Hereditary coproporphyria

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 65-90 Modifier:D046349 denotes hereditary coproporphyria
T2 99-124 SpecificDisease:D046349 denotes Hereditary coproporphyria
T3 126-129 SpecificDisease:D046349 denotes HCP
T4 137-163 DiseaseClass:D030342 denotes autosomal dominant disease
T5 183-223 SpecificDisease:D046349 denotes deficiency of coproporphyrinogen oxidase
T6 320-323 Modifier:D046349 denotes HCP

NCBI-Disease-Test

Id Subject Object Predicate Lexical cue database_id
T882 65-90 Modifier denotes hereditary coproporphyria D046349
T883 99-124 SpecificDisease denotes Hereditary coproporphyria D046349
T884 126-129 SpecificDisease denotes HCP D046349
T885 137-163 DiseaseClass denotes autosomal dominant disease D030342
T886 183-223 SpecificDisease denotes deficiency of coproporphyrinogen oxidase D046349
T887 320-323 Modifier denotes HCP D046349

NCBI-Disease-Test-Assistant-Knowledge

Id Subject Object Predicate Lexical cue
T1 65-90 CompositeMention denotes hereditary coproporphyria
T2 99-130 CompositeMention denotes Hereditary coproporphyria (HCP)
T3 156-163 DiseaseClass denotes disease
T4 197-229 SpecificDisease denotes coproporphyrinogen oxidase (CPO)
T5 320-332 CompositeMention denotes HCP patients

NCBI-Disease-Test-4o-NoGuidelineInPrompt

Id Subject Object Predicate Lexical cue
T1 65-90 SpecificDisease denotes hereditary coproporphyria
T2 99-130 SpecificDisease denotes Hereditary coproporphyria (HCP)
T3 156-163 DiseaseClass denotes disease
T4 320-323 SpecificDisease denotes HCP

NCBI-Disease-Corpus-o3-2

Id Subject Object Predicate Lexical cue
T1 65-90 Modifier denotes hereditary coproporphyria
T2 99-130 SpecificDisease denotes Hereditary coproporphyria (HCP)
T3 320-323 SpecificDisease denotes HCP

NCBI-Disease-Corpus-high-o3-1

Id Subject Object Predicate Lexical cue
T1 65-90 SpecificDisease denotes hereditary coproporphyria
T2 99-124 SpecificDisease denotes Hereditary coproporphyria
T3 126-129 SpecificDisease denotes HCP
T4 320-323 SpecificDisease denotes HCP

NCBI-Disease-Corpus-high-o3-2

Id Subject Object Predicate Lexical cue
T1 65-90 Modifier denotes hereditary coproporphyria
T2 99-124 SpecificDisease denotes Hereditary coproporphyria
T3 126-129 SpecificDisease denotes HCP
T4 320-323 Modifier denotes HCP

NCBI-Disease-Test-4o-GuidelineInPrompt

Id Subject Object Predicate Lexical cue
T1 65-90 Modifier denotes hereditary coproporphyria
T2 99-124 SpecificDisease denotes Hereditary coproporphyria
T3 137-163 DiseaseClass denotes autosomal dominant disease
T4 197-223 SpecificDisease denotes coproporphyrinogen oxidase
T5 320-323 Modifier denotes HCP

NCBI-Disease-Corpus-UpdatedGuideline

Id Subject Object Predicate Lexical cue
T1 65-90 DiseaseClass denotes hereditary coproporphyria
T2 99-124 SpecificDisease denotes Hereditary coproporphyria
T3 137-163 DiseaseClass denotes autosomal dominant disease
T4 320-323 SpecificDisease denotes HCP

NCBI-Disease-Corpus-humanintheloop

Id Subject Object Predicate Lexical cue
T1 65-90 Modifier denotes hereditary coproporphyria
T2 99-124 SpecificDisease denotes Hereditary coproporphyria
T3 320-323 Modifier denotes HCP

NCBI-Disease-Corpus-rezarta1

Id Subject Object Predicate Lexical cue
T1 65-90 Modifier denotes hereditary coproporphyria
T2 99-124 SpecificDisease denotes Hereditary coproporphyria
T3 320-323 SpecificDisease denotes HCP

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T882 65-90 Modifier denotes hereditary coproporphyria D046349
T883 99-124 SpecificDisease denotes Hereditary coproporphyria D046349
T884 126-129 SpecificDisease denotes HCP D046349
T885 137-163 DiseaseClass denotes autosomal dominant disease D030342
T886 183-223 SpecificDisease denotes deficiency of coproporphyrinogen oxidase D046349
T887 320-323 Modifier denotes HCP D046349

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 65-90 Modifier denotes hereditary coproporphyria
T2 99-124 SpecificDisease denotes Hereditary coproporphyria
T3 320-323 SpecificDisease denotes HCP

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 65-90 Modifier denotes hereditary coproporphyria
T2 99-124 SpecificDisease denotes Hereditary coproporphyria
T3 320-323 SpecificDisease denotes HCP

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 65-90 Modifier denotes hereditary coproporphyria
T2 99-124 SpecificDisease denotes Hereditary coproporphyria
T3 137-163 DiseaseClass denotes autosomal dominant disease
T4 197-223 SpecificDisease denotes coproporphyrinogen oxidase
T5 320-323 Modifier denotes HCP

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 65-90 SpecificDisease denotes hereditary coproporphyria
T2 99-130 SpecificDisease denotes Hereditary coproporphyria (HCP)
T3 197-229 Modifier denotes coproporphyrinogen oxidase (CPO)
T4 320-323 SpecificDisease denotes HCP

123456

Id Subject Object Predicate Lexical cue
T1 65-90 Modifier denotes hereditary coproporphyria
T2 99-124 SpecificDisease denotes Hereditary coproporphyria
T3 320-323 Modifier denotes HCP

12345

Id Subject Object Predicate Lexical cue
T1 65-90 Modifier denotes hereditary coproporphyria
T2 99-124 SpecificDisease denotes Hereditary coproporphyria
T3 126-129 SpecificDisease denotes HCP
T4 320-323 SpecificDisease denotes HCP