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NCBI-Disease-Corpus-GPT5-withguidelines

Id Subject Object Predicate Lexical cue
T1 7-26 SpecificDisease denotes early-onset obesity
T2 28-49 SpecificDisease denotes adrenal insufficiency
T3 389-413 SpecificDisease denotes isolated ACTH deficiency
T4 702-709 SpecificDisease denotes obesity
T5 821-828 SpecificDisease denotes obesity
T6 1001-1008 SpecificDisease denotes obesity
T7 1041-1056 SpecificDisease denotes ACTH deficiency
T8 1529-1557 DiseaseClass denotes monogenic endocrine disorder
T9 1571-1590 SpecificDisease denotes early-onset obesity
T10 1592-1613 SpecificDisease denotes adrenal insufficiency

NCBI-Disease-Corpus-GPT5-noguidelines

Id Subject Object Predicate Lexical cue
T1 0-75 CompositeMention denotes Severe early-onset obesity, adrenal insufficiency and red hair pigmentation
T2 389-397 Modifier denotes isolated
T3 398-413 SpecificDisease denotes ACTH deficiency
T4 702-709 SpecificDisease denotes obesity
T5 821-828 SpecificDisease denotes obesity
T6 899-916 DiseaseClass denotes hair pigmentation
T7 1001-1008 SpecificDisease denotes obesity
T8 1010-1036 DiseaseClass denotes alteration in pigmentation
T9 1041-1056 SpecificDisease denotes ACTH deficiency
T10 1529-1538 Modifier denotes monogenic
T11 1539-1557 DiseaseClass denotes endocrine disorder
T12 1571-1639 CompositeMention denotes early-onset obesity, adrenal insufficiency and red hair pigmentation

NCBI-Disease-Corpus-GPT5-guidelineprompt

Id Subject Object Predicate Lexical cue
T1 7-26 SpecificDisease denotes early-onset obesity
T2 28-49 SpecificDisease denotes adrenal insufficiency
T3 389-413 SpecificDisease denotes isolated ACTH deficiency
T4 702-709 SpecificDisease denotes obesity
T5 821-828 SpecificDisease denotes obesity
T6 1001-1008 SpecificDisease denotes obesity
T7 1041-1056 SpecificDisease denotes ACTH deficiency
T8 1529-1557 DiseaseClass denotes monogenic endocrine disorder
T9 1571-1590 SpecificDisease denotes early-onset obesity
T10 1592-1613 SpecificDisease denotes adrenal insufficiency

NCBI-Disease-Corpus-Moderated1

Id Subject Object Predicate Lexical cue
T1 19-26 SpecificDisease denotes obesity
T2 28-49 DiseaseClass denotes adrenal insufficiency
T3 389-413 SpecificDisease denotes isolated ACTH deficiency
T4 702-709 SpecificDisease denotes obesity
T5 821-828 SpecificDisease denotes obesity
T6 1001-1008 SpecificDisease denotes obesity
T7 1041-1056 SpecificDisease denotes ACTH deficiency
T8 1529-1557 DiseaseClass denotes monogenic endocrine disorder
T9 1583-1590 SpecificDisease denotes obesity
T10 1592-1613 DiseaseClass denotes adrenal insufficiency

DisGeNET

Id Subject Object Predicate Lexical cue
T0 565-574 gene:5443 denotes alpha-MSH
T1 702-709 disease:C0028754 denotes obesity
T2 565-574 gene:5443 denotes alpha-MSH
T3 821-828 disease:C0028754 denotes obesity
T4 635-658 gene:4160 denotes melanocortin-4-receptor
T5 702-709 disease:C0028754 denotes obesity
T6 635-658 gene:4160 denotes melanocortin-4-receptor
T7 821-828 disease:C0028754 denotes obesity
T8 660-665 gene:4160 denotes MC4-R
T9 702-709 disease:C0028754 denotes obesity
T10 660-665 gene:4160 denotes MC4-R
T11 821-828 disease:C0028754 denotes obesity
R1 T0 T1 associated_with alpha-MSH,obesity
R2 T2 T3 associated_with alpha-MSH,obesity
R3 T4 T5 associated_with melanocortin-4-receptor,obesity
R4 T6 T7 associated_with melanocortin-4-receptor,obesity
R5 T8 T9 associated_with MC4-R,obesity
R6 T10 T11 associated_with MC4-R,obesity

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
9620771-3#131#154#gene4160 635-658 gene4160 denotes melanocortin-4-receptor
9620771-3#156#161#gene4160 660-665 gene4160 denotes MC4-R
9620771-3#198#205#diseaseC0028754 702-709 diseaseC0028754 denotes obesity
9620771-3#317#324#diseaseC0028754 821-828 diseaseC0028754 denotes obesity
9620771-3#198#205#diseaseC0028754 702-709 diseaseC0028754 denotes obesity
9620771-3#317#324#diseaseC0028754 821-828 diseaseC0028754 denotes obesity
9620771-4#17#26#gene5443 847-856 gene5443 denotes alpha-MSH
9620771-4#211#226#diseaseC0342388 1041-1056 diseaseC0342388 denotes ACTH deficiency
9620771-8#75#79#gene5443 1502-1506 gene5443 denotes POMC
9620771-8#112#130#diseaseC0014130 1539-1557 diseaseC0014130 denotes endocrine disorder
9620771-8#156#163#diseaseC0028754 1583-1590 diseaseC0028754 denotes obesity
131#154#gene4160198#205#diseaseC0028754 9620771-3#131#154#gene4160 9620771-3#198#205#diseaseC0028754 associated_with melanocortin-4-receptor,obesity
131#154#gene4160317#324#diseaseC0028754 9620771-3#131#154#gene4160 9620771-3#317#324#diseaseC0028754 associated_with melanocortin-4-receptor,obesity
131#154#gene4160198#205#diseaseC0028754 9620771-3#131#154#gene4160 9620771-3#198#205#diseaseC0028754 associated_with melanocortin-4-receptor,obesity
131#154#gene4160317#324#diseaseC0028754 9620771-3#131#154#gene4160 9620771-3#317#324#diseaseC0028754 associated_with melanocortin-4-receptor,obesity
156#161#gene4160198#205#diseaseC0028754 9620771-3#156#161#gene4160 9620771-3#198#205#diseaseC0028754 associated_with MC4-R,obesity
156#161#gene4160317#324#diseaseC0028754 9620771-3#156#161#gene4160 9620771-3#317#324#diseaseC0028754 associated_with MC4-R,obesity
156#161#gene4160198#205#diseaseC0028754 9620771-3#156#161#gene4160 9620771-3#198#205#diseaseC0028754 associated_with MC4-R,obesity
156#161#gene4160317#324#diseaseC0028754 9620771-3#156#161#gene4160 9620771-3#317#324#diseaseC0028754 associated_with MC4-R,obesity
17#26#gene5443211#226#diseaseC0342388 9620771-4#17#26#gene5443 9620771-4#211#226#diseaseC0342388 associated_with alpha-MSH,ACTH deficiency
75#79#gene5443112#130#diseaseC0014130 9620771-8#75#79#gene5443 9620771-8#112#130#diseaseC0014130 associated_with POMC,endocrine disorder
75#79#gene5443156#163#diseaseC0028754 9620771-8#75#79#gene5443 9620771-8#156#163#diseaseC0028754 associated_with POMC,obesity

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 19-26 SpecificDisease:D009765 denotes obesity
T2 28-49 DiseaseClass:D000309 denotes adrenal insufficiency
T3 398-413 SpecificDisease:OMIM:201400|C535668 denotes ACTH deficiency
T4 702-709 SpecificDisease:D009765 denotes obesity
T5 821-828 SpecificDisease:D009765 denotes obesity
T6 1001-1008 SpecificDisease:D009765 denotes obesity
T7 1041-1056 SpecificDisease:OMIM:201400|C535668 denotes ACTH deficiency
T8 1476-1490 DiseaseClass:D030342 denotes genetic defect
T9 1529-1557 DiseaseClass:D004700 denotes monogenic endocrine disorder
T10 1583-1590 SpecificDisease:D009765 denotes obesity
T11 1592-1613 DiseaseClass:D000309 denotes adrenal insufficiency

NCBI-Disease-Test

Id Subject Object Predicate Lexical cue database_id
T835 19-26 SpecificDisease denotes obesity D009765
T836 28-49 DiseaseClass denotes adrenal insufficiency D000309
T837 398-413 SpecificDisease denotes ACTH deficiency OMIM:201400|C535668
T838 702-709 SpecificDisease denotes obesity D009765
T839 821-828 SpecificDisease denotes obesity D009765
T840 1001-1008 SpecificDisease denotes obesity D009765
T841 1041-1056 SpecificDisease denotes ACTH deficiency OMIM:201400|C535668
T842 1476-1490 DiseaseClass denotes genetic defect D030342
T843 1529-1557 DiseaseClass denotes monogenic endocrine disorder D004700
T844 1583-1590 SpecificDisease denotes obesity D009765
T845 1592-1613 DiseaseClass denotes adrenal insufficiency D000309

NCBI-Disease-Test-Assistant-Knowledge

Id Subject Object Predicate Lexical cue
T1 7-26 CompositeMention denotes early-onset obesity
T2 28-49 SpecificDisease denotes adrenal insufficiency
T3 54-75 Modifier denotes red hair pigmentation
T4 398-413 SpecificDisease denotes ACTH deficiency
T5 696-709 SpecificDisease denotes human obesity
T6 815-828 SpecificDisease denotes human obesity
T7 1001-1008 CompositeMention denotes obesity
T8 1041-1056 SpecificDisease denotes ACTH deficiency
T9 1571-1590 CompositeMention denotes early-onset obesity
T10 1592-1613 SpecificDisease denotes adrenal insufficiency
T11 1618-1639 Modifier denotes red hair pigmentation

NCBI-Disease-Test-4o-NoGuidelineInPrompt

Id Subject Object Predicate Lexical cue
T1 7-18 Modifier denotes early-onset
T2 19-26 SpecificDisease denotes obesity
T3 28-49 SpecificDisease denotes adrenal insufficiency
T4 54-75 SpecificDisease denotes red hair pigmentation
T5 86-100 CompositeMention denotes POMC mutations
T6 225-252 SpecificDisease denotes adrenocorticotrophin (ACTH)
T7 398-413 SpecificDisease denotes ACTH deficiency
T8 461-472 CompositeMention denotes POMC defect
T9 696-709 SpecificDisease denotes human obesity
T10 815-828 SpecificDisease denotes human obesity
T11 1001-1008 SpecificDisease denotes obesity
T12 1041-1056 SpecificDisease denotes ACTH deficiency
T13 1571-1582 Modifier denotes early-onset
T14 1583-1590 SpecificDisease denotes obesity
T15 1592-1613 SpecificDisease denotes adrenal insufficiency
T16 1618-1639 SpecificDisease denotes red hair pigmentation

NCBI-Disease-Corpus-o3-2

Id Subject Object Predicate Lexical cue
T1 0-26 SpecificDisease denotes Severe early-onset obesity
T2 28-49 SpecificDisease denotes adrenal insufficiency
T3 54-75 SpecificDisease denotes red hair pigmentation
T4 225-252 SpecificDisease denotes adrenocorticotrophin (ACTH)
T5 398-413 SpecificDisease denotes ACTH deficiency
T6 696-709 SpecificDisease denotes human obesity
T7 815-828 SpecificDisease denotes human obesity
T8 1001-1008 SpecificDisease denotes obesity
T9 1010-1036 SpecificDisease denotes alteration in pigmentation
T10 1041-1056 SpecificDisease denotes ACTH deficiency
T11 1523-1557 SpecificDisease denotes a new monogenic endocrine disorder
T12 1571-1590 SpecificDisease denotes early-onset obesity
T13 1592-1613 SpecificDisease denotes adrenal insufficiency
T14 1618-1639 SpecificDisease denotes red hair pigmentation

NCBI-Disease-Corpus-high-o3-1

Id Subject Object Predicate Lexical cue
T1 0-26 SpecificDisease denotes Severe early-onset obesity
T2 28-49 SpecificDisease denotes adrenal insufficiency
T3 54-75 SpecificDisease denotes red hair pigmentation
T4 389-413 SpecificDisease denotes isolated ACTH deficiency
T5 696-709 SpecificDisease denotes human obesity
T6 815-828 SpecificDisease denotes human obesity
T7 1001-1008 SpecificDisease denotes obesity
T8 1041-1056 SpecificDisease denotes ACTH deficiency
T9 1529-1557 DiseaseClass denotes monogenic endocrine disorder
T10 1571-1590 SpecificDisease denotes early-onset obesity
T11 1592-1613 SpecificDisease denotes adrenal insufficiency
T12 1618-1639 SpecificDisease denotes red hair pigmentation

NCBI-Disease-Corpus-high-o3-2

Id Subject Object Predicate Lexical cue
T1 0-26 SpecificDisease denotes Severe early-onset obesity
T2 28-49 SpecificDisease denotes adrenal insufficiency
T3 54-75 SpecificDisease denotes red hair pigmentation
T4 389-413 SpecificDisease denotes isolated ACTH deficiency
T5 696-709 SpecificDisease denotes human obesity
T6 815-828 SpecificDisease denotes human obesity
T7 1001-1008 SpecificDisease denotes obesity
T8 1041-1056 SpecificDisease denotes ACTH deficiency
T9 1529-1557 DiseaseClass denotes monogenic endocrine disorder
T10 1571-1590 SpecificDisease denotes early-onset obesity
T11 1592-1613 SpecificDisease denotes adrenal insufficiency
T12 1618-1639 SpecificDisease denotes red hair pigmentation

NCBI-Disease-Test-4o-GuidelineInPrompt

Id Subject Object Predicate Lexical cue
T1 7-26 SpecificDisease denotes early-onset obesity
T2 28-49 SpecificDisease denotes adrenal insufficiency
T3 225-252 SpecificDisease denotes adrenocorticotrophin (ACTH)
T4 398-413 SpecificDisease denotes ACTH deficiency
T5 696-709 Modifier denotes human obesity
T6 815-828 Modifier denotes human obesity
T7 1001-1008 SpecificDisease denotes obesity
T8 1041-1056 SpecificDisease denotes ACTH deficiency
T9 1571-1590 SpecificDisease denotes early-onset obesity
T10 1592-1613 SpecificDisease denotes adrenal insufficiency

NCBI-Disease-Corpus-UpdatedGuideline

Id Subject Object Predicate Lexical cue
T1 7-18 Modifier denotes early-onset
T2 19-26 SpecificDisease denotes obesity
T3 28-49 SpecificDisease denotes adrenal insufficiency
T4 54-62 Modifier denotes red hair
T5 86-100 SpecificDisease denotes POMC mutations
T6 225-252 SpecificDisease denotes adrenocorticotrophin (ACTH)
T7 398-413 SpecificDisease denotes ACTH deficiency
T8 461-472 SpecificDisease denotes POMC defect
T9 565-574 SpecificDisease denotes alpha-MSH
T10 696-709 SpecificDisease denotes human obesity
T11 815-828 SpecificDisease denotes human obesity
T12 847-856 SpecificDisease denotes alpha-MSH
T13 1001-1008 SpecificDisease denotes obesity
T14 1041-1056 SpecificDisease denotes ACTH deficiency
T15 1314-1318 SpecificDisease denotes ACTH
T16 1323-1332 SpecificDisease denotes alpha-MSH
T17 1539-1557 DiseaseClass denotes endocrine disorder
T18 1571-1582 Modifier denotes early-onset
T19 1583-1590 SpecificDisease denotes obesity
T20 1592-1613 SpecificDisease denotes adrenal insufficiency
T21 1618-1626 Modifier denotes red hair

NCBI-Disease-Corpus-humanintheloop

Id Subject Object Predicate Lexical cue
T1 19-26 SpecificDisease denotes obesity
T2 28-49 SpecificDisease denotes adrenal insufficiency
T3 225-245 SpecificDisease denotes adrenocorticotrophin
T4 247-251 SpecificDisease denotes ACTH
T5 287-290 SpecificDisease denotes MSH
T6 398-413 SpecificDisease denotes ACTH deficiency
T7 565-574 Modifier denotes alpha-MSH
T8 702-709 SpecificDisease denotes obesity
T9 821-828 SpecificDisease denotes obesity
T10 847-856 Modifier denotes alpha-MSH
T11 1001-1008 SpecificDisease denotes obesity
T12 1041-1056 SpecificDisease denotes ACTH deficiency
T13 1314-1318 Modifier denotes ACTH
T14 1323-1332 Modifier denotes alpha-MSH
T15 1571-1613 CompositeMention denotes early-onset obesity, adrenal insufficiency

NCBI-Disease-Corpus-rezarta1

Id Subject Object Predicate Lexical cue
T1 7-26 SpecificDisease denotes early-onset obesity
T2 28-49 SpecificDisease denotes adrenal insufficiency
T3 225-245 SpecificDisease denotes adrenocorticotrophin
T4 398-413 SpecificDisease denotes ACTH deficiency
T5 702-709 SpecificDisease denotes obesity
T6 821-828 SpecificDisease denotes obesity
T7 1001-1008 SpecificDisease denotes obesity
T8 1041-1056 SpecificDisease denotes ACTH deficiency
T9 1571-1590 SpecificDisease denotes early-onset obesity
T10 1592-1613 SpecificDisease denotes adrenal insufficiency

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T835 19-26 SpecificDisease denotes obesity D009765
T836 28-49 DiseaseClass denotes adrenal insufficiency D000309
T837 398-413 SpecificDisease denotes ACTH deficiency OMIM:201400|C535668
T838 702-709 SpecificDisease denotes obesity D009765
T839 821-828 SpecificDisease denotes obesity D009765
T840 1001-1008 SpecificDisease denotes obesity D009765
T841 1041-1056 SpecificDisease denotes ACTH deficiency OMIM:201400|C535668
T842 1476-1490 DiseaseClass denotes genetic defect D030342
T843 1529-1557 DiseaseClass denotes monogenic endocrine disorder D004700
T844 1583-1590 SpecificDisease denotes obesity D009765
T845 1592-1613 DiseaseClass denotes adrenal insufficiency D000309

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 19-26 SpecificDisease denotes obesity
T2 28-49 SpecificDisease denotes adrenal insufficiency
T3 225-245 Modifier denotes adrenocorticotrophin
T4 398-413 SpecificDisease denotes ACTH deficiency
T5 702-709 SpecificDisease denotes obesity
T6 821-828 SpecificDisease denotes obesity
T7 1001-1008 SpecificDisease denotes obesity
T8 1041-1056 SpecificDisease denotes ACTH deficiency
T9 1583-1590 SpecificDisease denotes obesity
T10 1592-1613 SpecificDisease denotes adrenal insufficiency

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 7-26 DiseaseClass denotes early-onset obesity
T2 28-49 SpecificDisease denotes adrenal insufficiency
T3 225-245 SpecificDisease denotes adrenocorticotrophin
T4 398-413 SpecificDisease denotes ACTH deficiency
T5 702-709 DiseaseClass denotes obesity
T6 821-828 DiseaseClass denotes obesity
T7 1001-1008 DiseaseClass denotes obesity
T8 1041-1056 SpecificDisease denotes ACTH deficiency
T9 1314-1318 Modifier denotes ACTH
T10 1571-1590 DiseaseClass denotes early-onset obesity
T11 1592-1613 SpecificDisease denotes adrenal insufficiency

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 7-75 CompositeMention denotes early-onset obesity, adrenal insufficiency and red hair pigmentation
T2 86-100 Modifier denotes POMC mutations
T3 247-251 SpecificDisease denotes ACTH
T4 398-413 SpecificDisease denotes ACTH deficiency
T5 461-472 Modifier denotes POMC defect
T6 702-709 SpecificDisease denotes obesity
T7 1001-1056 CompositeMention denotes obesity, alteration in pigmentation and ACTH deficiency
T8 1314-1318 SpecificDisease denotes ACTH
T9 1539-1557 SpecificDisease denotes endocrine disorder
T10 1571-1639 CompositeMention denotes early-onset obesity, adrenal insufficiency and red hair pigmentation

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 0-75 CompositeMention denotes Severe early-onset obesity, adrenal insufficiency and red hair pigmentation
T2 86-100 SpecificDisease denotes POMC mutations
T3 225-252 SpecificDisease denotes adrenocorticotrophin (ACTH)
T4 254-313 CompositeMention denotes melanocyte-stimulating hormones (MSH) alpha, beta and gamma
T5 352-366 SpecificDisease denotes beta-endorphin
T6 389-413 CompositeMention denotes isolated ACTH deficiency
T7 696-709 SpecificDisease denotes human obesity
T8 815-828 SpecificDisease denotes human obesity
T9 1001-1056 CompositeMention denotes obesity, alteration in pigmentation and ACTH deficiency
T10 1571-1639 CompositeMention denotes early-onset obesity, adrenal insufficiency and red hair pigmentation

123456

Id Subject Object Predicate Lexical cue
T12 1041-1056 SpecificDisease denotes ACTH deficiency
T13 1314-1318 Modifier denotes ACTH
T14 1323-1332 Modifier denotes alpha-MSH
T15 1571-1613 CompositeMention denotes early-onset obesity, adrenal insufficiency
T1 19-26 SpecificDisease denotes obesity
T2 28-49 SpecificDisease denotes adrenal insufficiency
T3 225-245 SpecificDisease denotes adrenocorticotrophin
T4 247-251 SpecificDisease denotes ACTH
T5 287-290 SpecificDisease denotes MSH
T6 398-413 SpecificDisease denotes ACTH deficiency
T7 565-574 Modifier denotes alpha-MSH
T8 702-709 SpecificDisease denotes obesity
T9 821-828 SpecificDisease denotes obesity
T10 847-856 Modifier denotes alpha-MSH
T11 1001-1008 SpecificDisease denotes obesity

12345

Id Subject Object Predicate Lexical cue
T1 7-49 CompositeMention denotes early-onset obesity, adrenal insufficiency
T2 225-252 DiseaseClass denotes adrenocorticotrophin (ACTH)
T3 398-413 SpecificDisease denotes ACTH deficiency
T4 702-709 SpecificDisease denotes obesity
T5 821-828 SpecificDisease denotes obesity
T6 1001-1008 SpecificDisease denotes obesity
T7 1041-1056 SpecificDisease denotes ACTH deficiency
T8 1314-1318 SpecificDisease denotes ACTH
T9 1571-1613 CompositeMention denotes early-onset obesity, adrenal insufficiency