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PubMed:9949209 JSONTXT

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NCBI-Disease-Corpus-GPT5-withguidelines

Id Subject Object Predicate Lexical cue
T1 23-39 Modifier denotes copper toxicosis
T2 158-185 DiseaseClass denotes hepatic copper accumulation
T3 272-299 DiseaseClass denotes hepatic copper accumulation
T4 346-360 SpecificDisease denotes Wilson disease
T5 362-364 SpecificDisease denotes WD
T6 499-522 DiseaseClass denotes copper overload disease
T7 523-553 SpecificDisease denotes non-Indian childhood cirrhosis
T8 637-653 SpecificDisease denotes copper toxicosis
T9 655-657 SpecificDisease denotes CT
T10 777-779 Modifier denotes WD
T11 814-816 SpecificDisease denotes CT
T12 999-1001 SpecificDisease denotes CT
T13 1147-1149 SpecificDisease denotes WD
T14 1174-1176 SpecificDisease denotes CT
T15 1261-1263 SpecificDisease denotes CT

NCBI-Disease-Corpus-GPT5-noguidelines

Id Subject Object Predicate Lexical cue
T1 23-39 SpecificDisease denotes copper toxicosis
T2 149-157 Modifier denotes Abnormal
T3 158-185 DiseaseClass denotes hepatic copper accumulation
T4 206-224 DiseaseClass denotes inherited disorder
T5 272-299 DiseaseClass denotes hepatic copper accumulation
T6 346-360 SpecificDisease denotes Wilson disease
T7 362-364 SpecificDisease denotes WD
T8 482-492 Modifier denotes much rarer
T9 499-522 DiseaseClass denotes copper overload disease
T10 523-553 SpecificDisease denotes non-Indian childhood cirrhosis
T11 610-616 Modifier denotes common
T12 617-636 Modifier denotes autosomal recessive
T13 637-653 SpecificDisease denotes copper toxicosis
T14 655-657 SpecificDisease denotes CT
T15 726-737 Modifier denotes progressive
T16 738-751 DiseaseClass denotes liver disease
T17 777-779 SpecificDisease denotes WD
T18 814-816 SpecificDisease denotes CT
T19 999-1001 SpecificDisease denotes CT
T20 1147-1149 SpecificDisease denotes WD
T21 1174-1176 SpecificDisease denotes CT
T22 1261-1263 SpecificDisease denotes CT

NCBI-Disease-Corpus-GPT5-guidelineprompt

Id Subject Object Predicate Lexical cue
T1 23-39 Modifier denotes copper toxicosis
T2 149-185 DiseaseClass denotes Abnormal hepatic copper accumulation
T3 272-299 DiseaseClass denotes hepatic copper accumulation
T4 346-360 SpecificDisease denotes Wilson disease
T5 362-364 SpecificDisease denotes WD
T6 499-522 Modifier denotes copper overload disease
T7 523-553 SpecificDisease denotes non-Indian childhood cirrhosis
T8 637-653 SpecificDisease denotes copper toxicosis
T9 655-657 SpecificDisease denotes CT
T10 777-779 Modifier denotes WD
T11 814-816 SpecificDisease denotes CT
T12 999-1001 SpecificDisease denotes CT
T13 1147-1149 SpecificDisease denotes WD
T14 1174-1176 SpecificDisease denotes CT
T15 1261-1263 SpecificDisease denotes CT

NCBI-Disease-Corpus-Moderated1

Id Subject Object Predicate Lexical cue
T1 23-39 Modifier denotes copper toxicosis
T2 206-224 DiseaseClass denotes inherited disorder
T3 346-360 SpecificDisease denotes Wilson disease
T4 362-364 SpecificDisease denotes WD
T5 493-522 DiseaseClass denotes human copper overload disease
T6 523-553 SpecificDisease denotes non-Indian childhood cirrhosis
T7 617-653 SpecificDisease denotes autosomal recessive copper toxicosis
T8 655-657 SpecificDisease denotes CT
T9 738-751 DiseaseClass denotes liver disease
T10 777-779 Modifier denotes WD
T11 814-816 SpecificDisease denotes CT
T12 999-1001 SpecificDisease denotes CT
T13 1147-1149 SpecificDisease denotes WD
T14 1174-1176 SpecificDisease denotes CT
T15 1214-1216 SpecificDisease denotes CT

DisGeNET

Id Subject Object Predicate Lexical cue
T0 326-331 gene:540 denotes ATP7B
T1 346-360 disease:C0019202 denotes Wilson disease
R1 T0 T1 associated_with ATP7B,Wilson disease

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
9949209-4#4#9#gene540 446-451 gene540 denotes ATP7B
9949209-4#85#111#diseaseC0268074 527-553 diseaseC0268074 denotes Indian childhood cirrhosis
9949209-8#31#36#gene540 1034-1039 gene540 denotes ATP7B
9949209-8#144#146#diseaseC0019202 1147-1149 diseaseC0019202 denotes WD
4#9#gene54085#111#diseaseC0268074 9949209-4#4#9#gene540 9949209-4#85#111#diseaseC0268074 associated_with ATP7B,Indian childhood cirrhosis
31#36#gene540144#146#diseaseC0019202 9949209-8#31#36#gene540 9949209-8#144#146#diseaseC0019202 associated_with ATP7B,WD

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 23-39 Modifier:OMIM:215600 denotes copper toxicosis
T2 158-185 SpecificDisease:D008107 denotes hepatic copper accumulation
T3 206-224 DiseaseClass:D030342 denotes inherited disorder
T4 272-299 SpecificDisease:D008107 denotes hepatic copper accumulation
T5 346-360 SpecificDisease:D006527 denotes Wilson disease
T6 362-364 SpecificDisease:D006527 denotes WD
T7 499-514 SpecificDisease:D008107 denotes copper overload
T8 523-553 SpecificDisease:OMIM:215600 denotes non-Indian childhood cirrhosis
T9 637-653 SpecificDisease:OMIM:215600 denotes copper toxicosis
T10 655-657 SpecificDisease:OMIM:215600 denotes CT
T11 738-751 DiseaseClass:D008107 denotes liver disease
T12 777-779 Modifier:D006527 denotes WD
T13 814-816 SpecificDisease:OMIM:215600 denotes CT
T14 999-1001 SpecificDisease:OMIM:215600 denotes CT
T15 1147-1149 SpecificDisease:D006527 denotes WD
T16 1174-1176 SpecificDisease:OMIM:215600 denotes CT
T17 1261-1263 SpecificDisease:OMIM:215600 denotes CT

NCBI-Disease-Test

Id Subject Object Predicate Lexical cue database_id
T1 23-39 Modifier denotes copper toxicosis OMIM:215600
T2 158-185 SpecificDisease denotes hepatic copper accumulation D008107
T3 206-224 DiseaseClass denotes inherited disorder D030342
T4 272-299 SpecificDisease denotes hepatic copper accumulation D008107
T5 346-360 SpecificDisease denotes Wilson disease D006527
T6 362-364 SpecificDisease denotes WD D006527
T7 499-514 SpecificDisease denotes copper overload D008107
T8 523-553 SpecificDisease denotes non-Indian childhood cirrhosis OMIM:215600
T9 637-653 SpecificDisease denotes copper toxicosis OMIM:215600
T10 655-657 SpecificDisease denotes CT OMIM:215600
T11 738-751 DiseaseClass denotes liver disease D008107
T12 777-779 Modifier denotes WD D006527
T13 814-816 SpecificDisease denotes CT OMIM:215600
T14 999-1001 SpecificDisease denotes CT OMIM:215600
T15 1147-1149 SpecificDisease denotes WD D006527
T16 1174-1176 SpecificDisease denotes CT OMIM:215600
T17 1261-1263 SpecificDisease denotes CT OMIM:215600

NCBI-Disease-Test-Assistant-Knowledge

Id Subject Object Predicate Lexical cue
T1 216-224 DiseaseClass denotes disorder
T2 272-299 CompositeMention denotes hepatic copper accumulation
T3 346-365 SpecificDisease denotes Wilson disease (WD)
T4 523-553 SpecificDisease denotes non-Indian childhood cirrhosis
T5 637-658 SpecificDisease denotes copper toxicosis (CT)
T6 726-751 CompositeMention denotes progressive liver disease

NCBI-Disease-Test-4o-NoGuidelineInPrompt

Id Subject Object Predicate Lexical cue
T1 216-224 SpecificDisease denotes disorder
T2 346-365 SpecificDisease denotes Wilson disease (WD)
T3 523-553 SpecificDisease denotes non-Indian childhood cirrhosis
T4 637-658 SpecificDisease denotes copper toxicosis (CT)
T5 726-751 CompositeMention denotes progressive liver disease
T6 777-779 SpecificDisease denotes WD
T7 814-816 SpecificDisease denotes CT
T8 999-1001 SpecificDisease denotes CT
T9 1147-1149 SpecificDisease denotes WD
T10 1174-1176 SpecificDisease denotes CT
T11 1261-1263 SpecificDisease denotes CT

NCBI-Disease-Corpus-o3-2

Id Subject Object Predicate Lexical cue
T1 23-39 SpecificDisease denotes copper toxicosis
T2 346-360 SpecificDisease denotes Wilson disease
T3 362-364 SpecificDisease denotes WD
T4 523-553 SpecificDisease denotes non-Indian childhood cirrhosis
T5 617-653 SpecificDisease denotes autosomal recessive copper toxicosis
T6 655-657 SpecificDisease denotes CT
T7 726-751 SpecificDisease denotes progressive liver disease
T8 814-816 SpecificDisease denotes CT
T9 999-1001 SpecificDisease denotes CT
T10 1147-1149 SpecificDisease denotes WD
T11 1174-1176 SpecificDisease denotes CT
T12 1261-1263 SpecificDisease denotes CT

NCBI-Disease-Corpus-high-o3-1

Id Subject Object Predicate Lexical cue
T1 23-39 SpecificDisease denotes copper toxicosis
T2 346-360 SpecificDisease denotes Wilson disease
T3 362-364 SpecificDisease denotes WD
T4 523-553 SpecificDisease denotes non-Indian childhood cirrhosis
T5 637-653 SpecificDisease denotes copper toxicosis
T6 655-657 SpecificDisease denotes CT
T7 726-751 DiseaseClass denotes progressive liver disease
T8 777-779 SpecificDisease denotes WD
T9 814-816 SpecificDisease denotes CT
T10 999-1001 SpecificDisease denotes CT
T11 1147-1149 SpecificDisease denotes WD
T12 1174-1176 SpecificDisease denotes CT
T13 1261-1263 SpecificDisease denotes CT

NCBI-Disease-Corpus-high-o3-2

Id Subject Object Predicate Lexical cue
T1 23-39 SpecificDisease denotes copper toxicosis
T2 346-360 SpecificDisease denotes Wilson disease
T3 362-364 SpecificDisease denotes WD
T4 637-653 SpecificDisease denotes copper toxicosis
T5 655-657 SpecificDisease denotes CT
T6 777-779 Modifier denotes WD
T7 814-816 SpecificDisease denotes CT
T8 999-1001 SpecificDisease denotes CT
T9 1147-1149 SpecificDisease denotes WD
T10 1174-1176 SpecificDisease denotes CT
T11 1261-1263 SpecificDisease denotes CT

NCBI-Disease-Test-4o-GuidelineInPrompt

Id Subject Object Predicate Lexical cue
T1 346-360 SpecificDisease denotes Wilson disease
T2 362-364 SpecificDisease denotes WD
T3 523-553 SpecificDisease denotes non-Indian childhood cirrhosis
T4 637-653 SpecificDisease denotes copper toxicosis
T5 655-657 SpecificDisease denotes CT
T6 726-751 DiseaseClass denotes progressive liver disease
T7 777-779 Modifier denotes WD
T8 814-816 Modifier denotes CT
T9 999-1001 Modifier denotes CT
T10 1147-1149 Modifier denotes WD
T11 1174-1176 Modifier denotes CT
T12 1261-1263 Modifier denotes CT

NCBI-Disease-Corpus-UpdatedGuideline

Id Subject Object Predicate Lexical cue
T1 216-224 DiseaseClass denotes disorder
T2 346-360 SpecificDisease denotes Wilson disease
T3 362-364 SpecificDisease denotes WD
T4 515-522 Modifier denotes disease
T5 523-553 SpecificDisease denotes non-Indian childhood cirrhosis
T6 617-653 DiseaseClass denotes autosomal recessive copper toxicosis
T7 655-657 SpecificDisease denotes CT
T8 726-751 DiseaseClass denotes progressive liver disease
T9 777-779 SpecificDisease denotes WD
T10 814-816 SpecificDisease denotes CT
T11 999-1001 SpecificDisease denotes CT
T12 1147-1149 SpecificDisease denotes WD
T13 1174-1176 SpecificDisease denotes CT
T14 1261-1263 SpecificDisease denotes CT

NCBI-Disease-Corpus-humanintheloop

Id Subject Object Predicate Lexical cue
T1 346-360 SpecificDisease denotes Wilson disease
T2 362-364 SpecificDisease denotes WD
T3 523-553 SpecificDisease denotes non-Indian childhood cirrhosis
T4 637-653 DiseaseClass denotes copper toxicosis
T5 655-657 SpecificDisease denotes CT
T6 738-751 SpecificDisease denotes liver disease
T7 777-779 Modifier denotes WD
T8 814-816 SpecificDisease denotes CT
T9 999-1001 SpecificDisease denotes CT
T10 1147-1149 Modifier denotes WD
T11 1174-1176 SpecificDisease denotes CT
T12 1261-1263 SpecificDisease denotes CT

NCBI-Disease-Corpus-rezarta1

Id Subject Object Predicate Lexical cue
T1 216-224 DiseaseClass denotes disorder
T2 272-299 SpecificDisease denotes hepatic copper accumulation
T3 346-360 SpecificDisease denotes Wilson disease
T4 362-364 SpecificDisease denotes WD
T5 515-522 DiseaseClass denotes disease
T6 523-553 SpecificDisease denotes non-Indian childhood cirrhosis
T7 637-653 DiseaseClass denotes copper toxicosis
T8 655-657 SpecificDisease denotes CT
T9 726-751 DiseaseClass denotes progressive liver disease
T10 777-779 Modifier denotes WD
T11 814-816 SpecificDisease denotes CT
T12 999-1001 SpecificDisease denotes CT
T13 1147-1149 SpecificDisease denotes WD
T14 1174-1176 SpecificDisease denotes CT
T15 1261-1263 SpecificDisease denotes CT

NCBI-Disease-Corpus-All

Id Subject Object Predicate Lexical cue database_id
T1 23-39 Modifier denotes copper toxicosis OMIM:215600
T2 158-185 SpecificDisease denotes hepatic copper accumulation D008107
T3 206-224 DiseaseClass denotes inherited disorder D030342
T4 272-299 SpecificDisease denotes hepatic copper accumulation D008107
T5 346-360 SpecificDisease denotes Wilson disease D006527
T6 362-364 SpecificDisease denotes WD D006527
T7 499-514 SpecificDisease denotes copper overload D008107
T8 523-553 SpecificDisease denotes non-Indian childhood cirrhosis OMIM:215600
T9 637-653 SpecificDisease denotes copper toxicosis OMIM:215600
T10 655-657 SpecificDisease denotes CT OMIM:215600
T11 738-751 DiseaseClass denotes liver disease D008107
T12 777-779 Modifier denotes WD D006527
T13 814-816 SpecificDisease denotes CT OMIM:215600
T14 999-1001 SpecificDisease denotes CT OMIM:215600
T15 1147-1149 SpecificDisease denotes WD D006527
T16 1174-1176 SpecificDisease denotes CT OMIM:215600
T17 1261-1263 SpecificDisease denotes CT OMIM:215600

NCBI-Disease-Corpus-2stage-All

Id Subject Object Predicate Lexical cue
T1 346-360 SpecificDisease denotes Wilson disease
T2 362-364 SpecificDisease denotes WD
T3 523-553 SpecificDisease denotes non-Indian childhood cirrhosis
T4 637-653 DiseaseClass denotes copper toxicosis
T5 655-657 SpecificDisease denotes CT
T6 738-751 DiseaseClass denotes liver disease
T7 777-779 Modifier denotes WD
T8 814-816 SpecificDisease denotes CT
T9 999-1001 SpecificDisease denotes CT
T10 1147-1149 SpecificDisease denotes WD
T11 1174-1176 SpecificDisease denotes CT
T12 1261-1263 SpecificDisease denotes CT

NCBI-Disease-Corpus-rezarta-All

Id Subject Object Predicate Lexical cue
T1 346-360 SpecificDisease denotes Wilson disease
T2 362-364 SpecificDisease denotes WD
T3 523-553 SpecificDisease denotes non-Indian childhood cirrhosis
T4 637-653 DiseaseClass denotes copper toxicosis
T5 655-657 SpecificDisease denotes CT
T6 726-751 DiseaseClass denotes progressive liver disease
T7 777-779 Modifier denotes WD
T8 814-816 SpecificDisease denotes CT
T9 999-1001 SpecificDisease denotes CT
T10 1147-1149 Modifier denotes WD
T11 1174-1176 SpecificDisease denotes CT
T12 1261-1263 SpecificDisease denotes CT

NCBI-Disease-Corpus-4oGuideline-All

Id Subject Object Predicate Lexical cue
T1 23-39 Modifier denotes copper toxicosis
T2 206-224 DiseaseClass denotes inherited disorder
T3 346-360 SpecificDisease denotes Wilson disease
T4 362-364 SpecificDisease denotes WD
T5 499-514 Modifier denotes copper overload
T6 523-553 SpecificDisease denotes non-Indian childhood cirrhosis
T7 617-653 DiseaseClass denotes autosomal recessive copper toxicosis
T8 655-657 Modifier denotes CT
T9 726-751 DiseaseClass denotes progressive liver disease
T10 814-816 Modifier denotes CT
T11 999-1001 Modifier denotes CT
T12 1147-1149 Modifier denotes WD
T13 1174-1176 Modifier denotes CT
T14 1261-1263 Modifier denotes CT

NCBI-Disease-Corpus-Simple-All

Id Subject Object Predicate Lexical cue
T1 216-224 SpecificDisease denotes disorder
T2 272-279 Modifier denotes hepatic
T3 346-365 SpecificDisease denotes Wilson disease (WD)
T4 515-522 SpecificDisease denotes disease
T5 523-553 SpecificDisease denotes non-Indian childhood cirrhosis
T6 637-658 CompositeMention denotes copper toxicosis (CT)
T7 726-737 Modifier denotes progressive
T8 738-751 SpecificDisease denotes liver disease

123456

Id Subject Object Predicate Lexical cue
T1 346-360 SpecificDisease denotes Wilson disease
T2 362-364 SpecificDisease denotes WD
T3 523-553 SpecificDisease denotes non-Indian childhood cirrhosis
T4 637-653 DiseaseClass denotes copper toxicosis
T5 655-657 SpecificDisease denotes CT
T6 738-751 SpecificDisease denotes liver disease
T7 777-779 Modifier denotes WD
T8 814-816 SpecificDisease denotes CT
T9 999-1001 SpecificDisease denotes CT
T10 1147-1149 Modifier denotes WD
T11 1174-1176 SpecificDisease denotes CT
T12 1261-1263 SpecificDisease denotes CT

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Id Subject Object Predicate Lexical cue
T1 216-224 DiseaseClass denotes disorder
T2 346-360 SpecificDisease denotes Wilson disease
T3 362-364 SpecificDisease denotes WD
T4 515-522 SpecificDisease denotes disease
T5 523-553 SpecificDisease denotes non-Indian childhood cirrhosis
T6 637-653 SpecificDisease denotes copper toxicosis
T7 655-657 SpecificDisease denotes CT
T8 738-751 DiseaseClass denotes liver disease
T9 777-779 Modifier denotes WD
T10 814-816 SpecificDisease denotes CT
T11 999-1001 SpecificDisease denotes CT
T12 1147-1149 SpecificDisease denotes WD
T13 1174-1176 SpecificDisease denotes CT
T14 1261-1263 SpecificDisease denotes CT