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NCBI-Disease-Corpus-GPT5-withguidelines

Id Subject Object Predicate Lexical cue
T1 89-124 SpecificDisease denotes autosomal recessive Alport syndrome
T2 126-161 SpecificDisease denotes Autosomal recessive Alport syndrome
T3 179-207 DiseaseClass denotes hematuric glomerulonephritis
T4 716-751 SpecificDisease denotes autosomal recessive Alport syndrome

NCBI-Disease-Corpus-GPT5-noguidelines

Id Subject Object Predicate Lexical cue
T1 89-124 SpecificDisease denotes autosomal recessive Alport syndrome
T2 126-161 SpecificDisease denotes Autosomal recessive Alport syndrome
T3 167-178 Modifier denotes progressive
T4 179-207 DiseaseClass denotes hematuric glomerulonephritis
T5 716-751 SpecificDisease denotes autosomal recessive Alport syndrome

NCBI-Disease-Corpus-GPT5-guidelineprompt

Id Subject Object Predicate Lexical cue
T1 89-124 SpecificDisease denotes autosomal recessive Alport syndrome
T2 126-161 SpecificDisease denotes Autosomal recessive Alport syndrome
T3 167-207 DiseaseClass denotes progressive hematuric glomerulonephritis
T4 716-751 SpecificDisease denotes autosomal recessive Alport syndrome

NCBI-Disease-Corpus-Moderated1

Id Subject Object Predicate Lexical cue
T1 89-124 SpecificDisease denotes autosomal recessive Alport syndrome
T2 126-161 SpecificDisease denotes Autosomal recessive Alport syndrome
T3 189-207 DiseaseClass denotes glomerulonephritis
T4 225-267 DiseaseClass denotes glomerular basement membrane abnormalities
T5 716-751 SpecificDisease denotes autosomal recessive Alport syndrome

DisGeNET

Id Subject Object Predicate Lexical cue
T0 312-318 gene:1285 denotes COL4A3
T1 189-207 disease:C0017658 denotes glomerulonephritis
T2 312-318 gene:1285 denotes COL4A3
T3 126-161 disease:C1567744 denotes Autosomal recessive Alport syndrome
T4 590-596 gene:1286 denotes COL4A4
T5 716-751 disease:C1567744 denotes autosomal recessive Alport syndrome
R1 T0 T1 associated_with COL4A3,glomerulonephritis
R2 T2 T3 associated_with COL4A3,Autosomal recessive Alport syndrome
R3 T4 T5 associated_with COL4A4,autosomal recessive Alport syndrome

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
9792860-0#46#52#gene1286 46-52 gene1286 denotes COL4A4
9792860-0#89#124#diseaseC1567744 89-124 diseaseC1567744 denotes autosomal recessive Alport syndrome
9792860-1#186#192#gene1285 312-318 gene1285 denotes COL4A3
9792860-1#0#35#diseaseC1567744 126-161 diseaseC1567744 denotes Autosomal recessive Alport syndrome
9792860-1#63#81#diseaseC0017658 189-207 diseaseC0017658 denotes glomerulonephritis
46#52#gene128689#124#diseaseC1567744 9792860-0#46#52#gene1286 9792860-0#89#124#diseaseC1567744 associated_with COL4A4,autosomal recessive Alport syndrome
186#192#gene12850#35#diseaseC1567744 9792860-1#186#192#gene1285 9792860-1#0#35#diseaseC1567744 associated_with COL4A3,Autosomal recessive Alport syndrome
186#192#gene128563#81#diseaseC0017658 9792860-1#186#192#gene1285 9792860-1#63#81#diseaseC0017658 associated_with COL4A3,glomerulonephritis

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 89-124 SpecificDisease:C536587 denotes autosomal recessive Alport syndrome
T2 126-161 SpecificDisease:C536587 denotes Autosomal recessive Alport syndrome
T3 179-207 SpecificDisease:D005921 denotes hematuric glomerulonephritis
T4 225-267 DiseaseClass:D005921 denotes glomerular basement membrane abnormalities
T5 716-751 SpecificDisease:C536587 denotes autosomal recessive Alport syndrome

NCBI-Disease-Test

Id Subject Object Predicate Lexical cue database_id
T263 89-124 SpecificDisease denotes autosomal recessive Alport syndrome C536587
T264 126-161 SpecificDisease denotes Autosomal recessive Alport syndrome C536587
T265 179-207 SpecificDisease denotes hematuric glomerulonephritis D005921
T266 225-267 DiseaseClass denotes glomerular basement membrane abnormalities D005921
T267 716-751 SpecificDisease denotes autosomal recessive Alport syndrome C536587

NCBI-Disease-Test-Assistant-Knowledge

Id Subject Object Predicate Lexical cue
T1 89-124 CompositeMention denotes autosomal recessive Alport syndrome
T2 126-161 CompositeMention denotes Autosomal recessive Alport syndrome
T3 179-207 DiseaseClass denotes hematuric glomerulonephritis
T4 716-751 CompositeMention denotes autosomal recessive Alport syndrome

NCBI-Disease-Test-4o-NoGuidelineInPrompt

Id Subject Object Predicate Lexical cue
T1 89-124 SpecificDisease denotes autosomal recessive Alport syndrome
T2 126-161 SpecificDisease denotes Autosomal recessive Alport syndrome
T3 179-207 DiseaseClass denotes hematuric glomerulonephritis
T4 716-751 SpecificDisease denotes autosomal recessive Alport syndrome

NCBI-Disease-Corpus-o3-2

Id Subject Object Predicate Lexical cue
T1 89-124 SpecificDisease denotes autosomal recessive Alport syndrome
T2 126-161 SpecificDisease denotes Autosomal recessive Alport syndrome
T3 179-207 SpecificDisease denotes hematuric glomerulonephritis
T4 716-751 SpecificDisease denotes autosomal recessive Alport syndrome

NCBI-Disease-Corpus-high-o3-1

Id Subject Object Predicate Lexical cue
T1 89-124 SpecificDisease denotes autosomal recessive Alport syndrome
T2 126-161 SpecificDisease denotes Autosomal recessive Alport syndrome
T3 167-207 SpecificDisease denotes progressive hematuric glomerulonephritis
T4 716-751 SpecificDisease denotes autosomal recessive Alport syndrome

NCBI-Disease-Corpus-high-o3-2

Id Subject Object Predicate Lexical cue
T1 89-124 SpecificDisease denotes autosomal recessive Alport syndrome
T2 126-161 SpecificDisease denotes Autosomal recessive Alport syndrome
T3 167-207 SpecificDisease denotes progressive hematuric glomerulonephritis
T4 716-751 SpecificDisease denotes autosomal recessive Alport syndrome

NCBI-Disease-Test-4o-GuidelineInPrompt

Id Subject Object Predicate Lexical cue
T1 89-124 SpecificDisease denotes autosomal recessive Alport syndrome
T2 126-161 SpecificDisease denotes Autosomal recessive Alport syndrome
T3 716-751 SpecificDisease denotes autosomal recessive Alport syndrome

NCBI-Disease-Corpus-UpdatedGuideline

Id Subject Object Predicate Lexical cue
T1 89-124 DiseaseClass denotes autosomal recessive Alport syndrome
T2 126-161 DiseaseClass denotes Autosomal recessive Alport syndrome
T3 179-207 SpecificDisease denotes hematuric glomerulonephritis
T4 716-751 DiseaseClass denotes autosomal recessive Alport syndrome

NCBI-Disease-Corpus-humanintheloop

Id Subject Object Predicate Lexical cue
T1 89-124 SpecificDisease denotes autosomal recessive Alport syndrome
T2 126-161 SpecificDisease denotes Autosomal recessive Alport syndrome
T3 189-207 DiseaseClass denotes glomerulonephritis
T4 716-751 SpecificDisease denotes autosomal recessive Alport syndrome

NCBI-Disease-Corpus-rezarta1

Id Subject Object Predicate Lexical cue
T1 89-124 SpecificDisease denotes autosomal recessive Alport syndrome
T2 126-161 SpecificDisease denotes Autosomal recessive Alport syndrome
T3 189-207 SpecificDisease denotes glomerulonephritis
T4 716-751 SpecificDisease denotes autosomal recessive Alport syndrome

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T263 89-124 SpecificDisease denotes autosomal recessive Alport syndrome C536587
T264 126-161 SpecificDisease denotes Autosomal recessive Alport syndrome C536587
T265 179-207 SpecificDisease denotes hematuric glomerulonephritis D005921
T266 225-267 DiseaseClass denotes glomerular basement membrane abnormalities D005921
T267 716-751 SpecificDisease denotes autosomal recessive Alport syndrome C536587

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 89-124 SpecificDisease denotes autosomal recessive Alport syndrome
T2 126-161 SpecificDisease denotes Autosomal recessive Alport syndrome
T3 716-751 SpecificDisease denotes autosomal recessive Alport syndrome

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 89-124 SpecificDisease denotes autosomal recessive Alport syndrome
T2 126-161 SpecificDisease denotes Autosomal recessive Alport syndrome
T3 189-207 SpecificDisease denotes glomerulonephritis
T4 716-751 SpecificDisease denotes autosomal recessive Alport syndrome

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 89-124 SpecificDisease denotes autosomal recessive Alport syndrome
T2 126-161 SpecificDisease denotes Autosomal recessive Alport syndrome
T3 189-207 SpecificDisease denotes glomerulonephritis
T4 716-751 SpecificDisease denotes autosomal recessive Alport syndrome

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 89-124 SpecificDisease denotes autosomal recessive Alport syndrome
T2 126-161 SpecificDisease denotes Autosomal recessive Alport syndrome
T3 179-207 CompositeMention denotes hematuric glomerulonephritis
T4 716-751 SpecificDisease denotes autosomal recessive Alport syndrome

123456

Id Subject Object Predicate Lexical cue
T1 89-124 SpecificDisease denotes autosomal recessive Alport syndrome
T2 126-161 SpecificDisease denotes Autosomal recessive Alport syndrome
T3 189-207 DiseaseClass denotes glomerulonephritis
T4 716-751 SpecificDisease denotes autosomal recessive Alport syndrome

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Id Subject Object Predicate Lexical cue
T1 89-124 Modifier denotes autosomal recessive Alport syndrome
T2 126-161 SpecificDisease denotes Autosomal recessive Alport syndrome
T3 189-207 SpecificDisease denotes glomerulonephritis
T4 716-751 SpecificDisease denotes autosomal recessive Alport syndrome