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NCBI-Disease-Corpus-GPT5-withguidelines

Id	Subject	Object	Predicate	Lexical cue
T1	30-47	Modifier	denotes	Angelman syndrome
T2	58-75	SpecificDisease	denotes	Angelman syndrome
T3	77-79	SpecificDisease	denotes	AS
T4	402-404	Modifier	denotes	AS
T5	981-983	Modifier	denotes	AS
T6	1025-1027	Modifier	denotes	AS
T7	1067-1069	Modifier	denotes	AS

NCBI-Disease-Corpus-GPT5-noguidelines

Id	Subject	Object	Predicate	Lexical cue
T1	30-47	SpecificDisease	denotes	Angelman syndrome
T2	58-75	SpecificDisease	denotes	Angelman syndrome
T3	77-79	SpecificDisease	denotes	AS
T4	402-404	SpecificDisease	denotes	AS
T5	444-451	Modifier	denotes	de novo
T6	835-843	Modifier	denotes	familial
T7	859-867	Modifier	denotes	sporadic
T8	876-884	Modifier	denotes	familial
T9	899-907	Modifier	denotes	sporadic
T10	914-923	Modifier	denotes	mosaicism
T11	981-983	SpecificDisease	denotes	AS
T12	1025-1027	SpecificDisease	denotes	AS
T13	1067-1069	SpecificDisease	denotes	AS
T14	1151-1159	Modifier	denotes	sporadic
T15	1187-1195	Modifier	denotes	familial

NCBI-Disease-Corpus-GPT5-guidelineprompt

Id	Subject	Object	Predicate	Lexical cue
T1	30-47	Modifier	denotes	Angelman syndrome
T2	58-75	SpecificDisease	denotes	Angelman syndrome
T3	77-79	SpecificDisease	denotes	AS
T4	402-404	Modifier	denotes	AS
T5	981-983	Modifier	denotes	AS
T6	1025-1027	Modifier	denotes	AS
T7	1067-1069	Modifier	denotes	AS

NCBI-Disease-Corpus-Moderated1

Id	Subject	Object	Predicate	Lexical cue
T1	30-47	Modifier	denotes	Angelman syndrome
T2	77-79	SpecificDisease	denotes	AS
T3	94-143	DiseaseClass	denotes	chromosome 15q11-q13 deletions of maternal origin
T4	148-175	DiseaseClass	denotes	paternal uniparental disomy
T5	177-180	DiseaseClass	denotes	UPD
T6	402-404	Modifier	denotes	AS
T7	981-983	Modifier	denotes	AS
T8	1025-1027	Modifier	denotes	AS

DisGeNET

Id	Subject	Object	Predicate	Lexical cue
T0	21-26	gene:7337	denotes	UBE3A
T1	30-47	disease:C0162635	denotes	Angelman syndrome
R1	T0	T1	associated_with	UBE3A,Angelman syndrome

DisGeNET5_gene_disease

Id	Subject	Object	Predicate	Lexical cue
9585605-0#21#26#gene7337	21-26	gene7337	denotes	UBE3A
9585605-0#30#47#diseaseC0162635	30-47	diseaseC0162635	denotes	Angelman syndrome
21#26#gene733730#47#diseaseC0162635	9585605-0#21#26#gene7337	9585605-0#30#47#diseaseC0162635	associated_with	UBE3A,Angelman syndrome

NCBIDiseaseCorpus

Id	Subject	Object	Predicate	Lexical cue
T1	30-47	Modifier:D017204	denotes	Angelman syndrome
T2	58-75	SpecificDisease:D017204	denotes	Angelman syndrome
T3	77-79	SpecificDisease:D017204	denotes	AS
T4	157-175	SpecificDisease:D024182	denotes	uniparental disomy
T5	177-180	SpecificDisease:D024182	denotes	UPD
T6	402-404	Modifier:D017204	denotes	AS
T7	981-983	Modifier:D017204	denotes	AS
T8	1025-1027	Modifier:D017204	denotes	AS
T9	1067-1069	Modifier:D017204	denotes	AS

NCBI-Disease-Test

Id	Subject	Object	Predicate	Lexical cue	database_id
T414	30-47	Modifier	denotes	Angelman syndrome	D017204
T415	58-75	SpecificDisease	denotes	Angelman syndrome	D017204
T416	77-79	SpecificDisease	denotes	AS	D017204
T417	157-175	SpecificDisease	denotes	uniparental disomy	D024182
T418	177-180	SpecificDisease	denotes	UPD	D024182
T419	402-404	Modifier	denotes	AS	D017204
T420	981-983	Modifier	denotes	AS	D017204
T421	1025-1027	Modifier	denotes	AS	D017204
T422	1067-1069	Modifier	denotes	AS	D017204

NCBI-Disease-Test-Assistant-Knowledge

Id	Subject	Object	Predicate	Lexical cue
T1	21-26	SpecificDisease	denotes	UBE3A
T2	30-47	SpecificDisease	denotes	Angelman syndrome
T3	58-80	SpecificDisease	denotes	Angelman syndrome (AS)
T4	233-238	SpecificDisease	denotes	UBE3A
T5	245-250	SpecificDisease	denotes	UBE3A
T6	340-345	SpecificDisease	denotes	UBE3A
T7	402-404	SpecificDisease	denotes	AS
T8	742-747	SpecificDisease	denotes	UBE3A
T9	928-933	SpecificDisease	denotes	UBE3A
T10	981-983	SpecificDisease	denotes	AS
T11	1025-1027	SpecificDisease	denotes	AS
T12	1067-1069	SpecificDisease	denotes	AS

NCBI-Disease-Test-4o-NoGuidelineInPrompt

Id	Subject	Object	Predicate	Lexical cue
T1	30-47	SpecificDisease	denotes	Angelman syndrome
T2	58-80	SpecificDisease	denotes	Angelman syndrome (AS)
T3	402-404	SpecificDisease	denotes	AS
T4	981-983	SpecificDisease	denotes	AS
T5	1025-1027	SpecificDisease	denotes	AS
T6	1067-1069	SpecificDisease	denotes	AS

NCBI-Disease-Corpus-o3-2

Id	Subject	Object	Predicate	Lexical cue
T1	30-47	Modifier	denotes	Angelman syndrome
T2	58-75	SpecificDisease	denotes	Angelman syndrome
T3	77-79	SpecificDisease	denotes	AS
T4	402-404	Modifier	denotes	AS
T5	981-983	Modifier	denotes	AS
T6	1025-1027	Modifier	denotes	AS
T7	1067-1069	Modifier	denotes	AS

NCBI-Disease-Corpus-high-o3-1

Id	Subject	Object	Predicate	Lexical cue
T1	30-47	Modifier	denotes	Angelman syndrome
T2	58-75	SpecificDisease	denotes	Angelman syndrome
T3	77-79	SpecificDisease	denotes	AS
T4	402-404	Modifier	denotes	AS
T5	981-983	Modifier	denotes	AS
T6	1025-1027	Modifier	denotes	AS
T7	1067-1069	Modifier	denotes	AS

NCBI-Disease-Corpus-high-o3-2

Id	Subject	Object	Predicate	Lexical cue
T1	30-47	Modifier	denotes	Angelman syndrome
T2	58-75	SpecificDisease	denotes	Angelman syndrome
T3	77-79	SpecificDisease	denotes	AS
T4	402-404	Modifier	denotes	AS
T5	981-983	Modifier	denotes	AS
T6	1025-1027	Modifier	denotes	AS
T7	1067-1069	Modifier	denotes	AS

NCBI-Disease-Test-4o-GuidelineInPrompt

Id	Subject	Object	Predicate	Lexical cue
T1	30-47	SpecificDisease	denotes	Angelman syndrome
T2	58-75	SpecificDisease	denotes	Angelman syndrome
T3	77-79	SpecificDisease	denotes	AS
T4	402-404	SpecificDisease	denotes	AS
T5	981-983	SpecificDisease	denotes	AS
T6	1025-1027	SpecificDisease	denotes	AS
T7	1067-1069	SpecificDisease	denotes	AS

NCBI-Disease-Corpus-UpdatedGuideline

Id	Subject	Object	Predicate	Lexical cue
T1	30-47	SpecificDisease	denotes	Angelman syndrome
T2	58-75	SpecificDisease	denotes	Angelman syndrome
T3	77-79	SpecificDisease	denotes	AS
T4	402-404	SpecificDisease	denotes	AS
T5	981-983	SpecificDisease	denotes	AS
T6	1025-1027	SpecificDisease	denotes	AS
T7	1067-1069	SpecificDisease	denotes	AS

NCBI-Disease-Corpus-humanintheloop

Id	Subject	Object	Predicate	Lexical cue
T1	30-47	Modifier	denotes	Angelman syndrome
T2	58-75	SpecificDisease	denotes	Angelman syndrome
T3	77-79	SpecificDisease	denotes	AS
T4	402-404	Modifier	denotes	AS
T5	981-983	Modifier	denotes	AS
T6	1025-1027	Modifier	denotes	AS
T7	1067-1069	Modifier	denotes	AS

NCBI-Disease-Corpus-rezarta1

Id	Subject	Object	Predicate	Lexical cue
T1	30-47	Modifier	denotes	Angelman syndrome
T2	58-75	SpecificDisease	denotes	Angelman syndrome
T3	77-79	SpecificDisease	denotes	AS
T4	402-404	Modifier	denotes	AS
T5	981-983	Modifier	denotes	AS
T6	1025-1027	Modifier	denotes	AS
T7	1067-1069	Modifier	denotes	AS

NCBI-Disease-Corpus-All

Id	Subject	Object	Predicate	Lexical cue	database_id
T414	30-47	Modifier	denotes	Angelman syndrome	D017204
T415	58-75	SpecificDisease	denotes	Angelman syndrome	D017204
T416	77-79	SpecificDisease	denotes	AS	D017204
T417	157-175	SpecificDisease	denotes	uniparental disomy	D024182
T418	177-180	SpecificDisease	denotes	UPD	D024182
T419	402-404	Modifier	denotes	AS	D017204
T420	981-983	Modifier	denotes	AS	D017204
T421	1025-1027	Modifier	denotes	AS	D017204
T422	1067-1069	Modifier	denotes	AS	D017204

NCBI-Disease-Corpus-2stage-All

Id	Subject	Object	Predicate	Lexical cue
T1	30-47	Modifier	denotes	Angelman syndrome
T2	58-75	SpecificDisease	denotes	Angelman syndrome
T3	77-79	SpecificDisease	denotes	AS
T4	402-404	Modifier	denotes	AS
T5	981-983	Modifier	denotes	AS
T6	1025-1027	Modifier	denotes	AS
T7	1067-1069	Modifier	denotes	AS

NCBI-Disease-Corpus-rezarta-All

Id	Subject	Object	Predicate	Lexical cue
T1	30-47	Modifier	denotes	Angelman syndrome
T2	58-75	SpecificDisease	denotes	Angelman syndrome
T3	77-79	SpecificDisease	denotes	AS
T4	402-404	Modifier	denotes	AS
T5	981-983	Modifier	denotes	AS
T6	1025-1027	Modifier	denotes	AS
T7	1067-1069	Modifier	denotes	AS

NCBI-Disease-Corpus-4oGuideline-All

Id	Subject	Object	Predicate	Lexical cue
T1	21-26	SpecificDisease	denotes	UBE3A
T2	30-47	SpecificDisease	denotes	Angelman syndrome
T3	58-75	SpecificDisease	denotes	Angelman syndrome
T4	77-79	SpecificDisease	denotes	AS
T5	233-238	SpecificDisease	denotes	UBE3A
T6	245-250	SpecificDisease	denotes	UBE3A
T7	340-345	SpecificDisease	denotes	UBE3A
T8	402-404	SpecificDisease	denotes	AS
T9	742-747	SpecificDisease	denotes	UBE3A
T10	928-933	SpecificDisease	denotes	UBE3A
T11	981-983	SpecificDisease	denotes	AS
T12	1025-1027	SpecificDisease	denotes	AS
T13	1067-1069	SpecificDisease	denotes	AS

NCBI-Disease-Corpus-Simple-All

Id	Subject	Object	Predicate	Lexical cue
T1	30-47	SpecificDisease	denotes	Angelman syndrome
T2	58-80	SpecificDisease	denotes	Angelman syndrome (AS)
T3	148-184	CompositeMention	denotes	paternal uniparental disomy (UPD) 15

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Id	Subject	Object	Predicate	Lexical cue
T1	30-47	Modifier	denotes	Angelman syndrome
T2	58-75	SpecificDisease	denotes	Angelman syndrome
T3	77-79	SpecificDisease	denotes	AS
T4	402-404	Modifier	denotes	AS
T5	981-983	Modifier	denotes	AS
T6	1025-1027	Modifier	denotes	AS
T7	1067-1069	Modifier	denotes	AS

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Id	Subject	Object	Predicate	Lexical cue
T1	30-47	Modifier	denotes	Angelman syndrome
T2	58-75	SpecificDisease	denotes	Angelman syndrome
T3	77-79	SpecificDisease	denotes	AS
T4	402-404	Modifier	denotes	AS
T5	981-983	Modifier	denotes	AS
T6	1025-1027	Modifier	denotes	AS
T7	1067-1069	Modifier	denotes	AS