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NCBI-Disease-Corpus-GPT5-withguidelines

Id	Subject	Object	Predicate	Lexical cue
T1	35-51	SpecificDisease	denotes	Pendred syndrome
T2	76-104	DiseaseClass	denotes	autosomal recessive disorder
T3	138-157	CompositeMention	denotes	deafness and goiter
T4	416-423	Modifier	denotes	Pendred
T5	894-901	Modifier	denotes	Pendred
T6	1190-1206	SpecificDisease	denotes	Pendred syndrome

NCBI-Disease-Corpus-GPT5-noguidelines

Id	Subject	Object	Predicate	Lexical cue
T1	35-51	SpecificDisease	denotes	Pendred syndrome
T2	76-104	DiseaseClass	denotes	autosomal recessive disorder
T3	122-137	Modifier	denotes	early childhood
T4	138-146	SpecificDisease	denotes	deafness
T5	151-157	SpecificDisease	denotes	goiter
T6	196-204	DiseaseClass	denotes	syndrome
T7	1190-1206	SpecificDisease	denotes	Pendred syndrome

NCBI-Disease-Corpus-GPT5-guidelineprompt

Id	Subject	Object	Predicate	Lexical cue
T1	35-51	SpecificDisease	denotes	Pendred syndrome
T2	76-104	DiseaseClass	denotes	autosomal recessive disorder
T3	122-157	CompositeMention	denotes	early childhood deafness and goiter
T4	416-423	Modifier	denotes	Pendred
T5	894-901	Modifier	denotes	Pendred
T6	1190-1206	SpecificDisease	denotes	Pendred syndrome

NCBI-Disease-Corpus-Moderated1

Id	Subject	Object	Predicate	Lexical cue
T1	35-51	SpecificDisease	denotes	Pendred syndrome
T2	76-104	DiseaseClass	denotes	autosomal recessive disorder
T3	138-157	CompositeMention	denotes	deafness and goiter
T4	416-423	Modifier	denotes	Pendred
T5	894-901	Modifier	denotes	Pendred
T6	1190-1206	SpecificDisease	denotes	Pendred syndrome

DisGeNET

Id	Subject	Object	Predicate	Lexical cue
T0	1133-1136	gene:5172	denotes	PDS
T1	1190-1206	disease:C0271829	denotes	Pendred syndrome
T2	1133-1136	gene:5730	denotes	PDS
T3	1190-1206	disease:C0271829	denotes	Pendred syndrome
R1	T0	T1	associated_with	PDS,Pendred syndrome
R2	T2	T3	associated_with	PDS,Pendred syndrome

NCBIDiseaseCorpus

Id	Subject	Object	Predicate	Lexical cue
T1	35-51	SpecificDisease:C536648	denotes	Pendred syndrome
T2	53-69	SpecificDisease:C536648	denotes	Pendred syndrome
T3	76-104	DiseaseClass:D030342	denotes	autosomal recessive disorder
T4	138-146	SpecificDisease:D003638	denotes	deafness
T5	151-157	SpecificDisease:D006042	denotes	goiter
T6	387-390	Modifier:C536648	denotes	PDS
T7	416-423	Modifier:C536648	denotes	Pendred
T8	894-901	Modifier:C536648	denotes	Pendred
T9	1133-1136	Modifier:C536648	denotes	PDS
T10	1190-1206	SpecificDisease:C536648	denotes	Pendred syndrome

NCBI-Disease-Test

Id	Subject	Object	Predicate	Lexical cue	database_id
T195	35-51	SpecificDisease	denotes	Pendred syndrome	C536648
T196	53-69	SpecificDisease	denotes	Pendred syndrome	C536648
T197	76-104	DiseaseClass	denotes	autosomal recessive disorder	D030342
T198	138-146	SpecificDisease	denotes	deafness	D003638
T199	151-157	SpecificDisease	denotes	goiter	D006042
T200	387-390	Modifier	denotes	PDS	C536648
T201	416-423	Modifier	denotes	Pendred	C536648
T202	894-901	Modifier	denotes	Pendred	C536648
T203	1133-1136	Modifier	denotes	PDS	C536648
T204	1190-1206	SpecificDisease	denotes	Pendred syndrome	C536648

NCBI-Disease-Test-Assistant-Knowledge

Id	Subject	Object	Predicate	Lexical cue
T1	35-51	SpecificDisease	denotes	Pendred syndrome
T2	53-69	SpecificDisease	denotes	Pendred syndrome
T3	138-146	SpecificDisease	denotes	deafness
T4	151-157	SpecificDisease	denotes	goiter
T5	416-423	SpecificDisease	denotes	Pendred
T6	894-901	SpecificDisease	denotes	Pendred
T7	1190-1206	SpecificDisease	denotes	Pendred syndrome

NCBI-Disease-Test-4o-NoGuidelineInPrompt

Id	Subject	Object	Predicate	Lexical cue
T1	35-51	SpecificDisease	denotes	Pendred syndrome
T2	53-69	SpecificDisease	denotes	Pendred syndrome
T3	138-146	SpecificDisease	denotes	deafness
T4	151-157	SpecificDisease	denotes	goiter
T5	229-249	CompositeMention	denotes	disease gene ( PDS )
T6	387-395	CompositeMention	denotes	PDS gene
T7	416-423	SpecificDisease	denotes	Pendred
T8	894-901	SpecificDisease	denotes	Pendred
T9	1133-1146	CompositeMention	denotes	PDS mutations
T10	1190-1206	SpecificDisease	denotes	Pendred syndrome

NCBI-Disease-Corpus-o3-2

Id	Subject	Object	Predicate	Lexical cue
T1	35-51	SpecificDisease	denotes	Pendred syndrome
T2	53-69	SpecificDisease	denotes	Pendred syndrome
T3	76-104	DiseaseClass	denotes	autosomal recessive disorder
T4	122-146	SpecificDisease	denotes	early childhood deafness
T5	151-157	SpecificDisease	denotes	goiter
T6	416-423	Modifier	denotes	Pendred
T7	894-901	Modifier	denotes	Pendred
T8	1190-1206	SpecificDisease	denotes	Pendred syndrome

NCBI-Disease-Corpus-high-o3-1

Id	Subject	Object	Predicate	Lexical cue
T1	35-51	SpecificDisease	denotes	Pendred syndrome
T2	53-69	SpecificDisease	denotes	Pendred syndrome
T3	1190-1206	SpecificDisease	denotes	Pendred syndrome

NCBI-Disease-Corpus-high-o3-2

Id	Subject	Object	Predicate	Lexical cue
T1	35-51	SpecificDisease	denotes	Pendred syndrome
T2	53-69	SpecificDisease	denotes	Pendred syndrome
T3	1190-1206	SpecificDisease	denotes	Pendred syndrome

NCBI-Disease-Test-4o-GuidelineInPrompt

Id	Subject	Object	Predicate	Lexical cue
T1	35-51	SpecificDisease	denotes	Pendred syndrome
T2	53-69	SpecificDisease	denotes	Pendred syndrome
T3	416-423	SpecificDisease	denotes	Pendred
T4	894-901	SpecificDisease	denotes	Pendred
T5	1190-1206	SpecificDisease	denotes	Pendred syndrome

NCBI-Disease-Corpus-UpdatedGuideline

Id	Subject	Object	Predicate	Lexical cue
T1	35-51	SpecificDisease	denotes	Pendred syndrome
T2	53-69	SpecificDisease	denotes	Pendred syndrome
T3	76-104	DiseaseClass	denotes	autosomal recessive disorder
T4	894-901	Modifier	denotes	Pendred
T5	1190-1206	SpecificDisease	denotes	Pendred syndrome

NCBI-Disease-Corpus-humanintheloop

Id	Subject	Object	Predicate	Lexical cue
T1	35-51	SpecificDisease	denotes	Pendred syndrome
T2	53-69	SpecificDisease	denotes	Pendred syndrome
T3	151-157	DiseaseClass	denotes	goiter
T4	416-423	Modifier	denotes	Pendred
T5	894-901	Modifier	denotes	Pendred
T6	1190-1206	SpecificDisease	denotes	Pendred syndrome

NCBI-Disease-Corpus-rezarta1

Id	Subject	Object	Predicate	Lexical cue
T1	35-51	SpecificDisease	denotes	Pendred syndrome
T2	53-69	SpecificDisease	denotes	Pendred syndrome
T3	416-423	Modifier	denotes	Pendred
T4	894-901	Modifier	denotes	Pendred
T5	1190-1206	SpecificDisease	denotes	Pendred syndrome

NCBI-Disease-Corpus-All

Id	Subject	Object	Predicate	Lexical cue	database_id
T195	35-51	SpecificDisease	denotes	Pendred syndrome	C536648
T196	53-69	SpecificDisease	denotes	Pendred syndrome	C536648
T197	76-104	DiseaseClass	denotes	autosomal recessive disorder	D030342
T198	138-146	SpecificDisease	denotes	deafness	D003638
T199	151-157	SpecificDisease	denotes	goiter	D006042
T200	387-390	Modifier	denotes	PDS	C536648
T201	416-423	Modifier	denotes	Pendred	C536648
T202	894-901	Modifier	denotes	Pendred	C536648
T203	1133-1136	Modifier	denotes	PDS	C536648
T204	1190-1206	SpecificDisease	denotes	Pendred syndrome	C536648

NCBI-Disease-Corpus-2stage-All

Id	Subject	Object	Predicate	Lexical cue
T1	35-51	SpecificDisease	denotes	Pendred syndrome
T2	53-69	SpecificDisease	denotes	Pendred syndrome
T3	416-423	Modifier	denotes	Pendred
T4	894-901	Modifier	denotes	Pendred
T5	1190-1206	SpecificDisease	denotes	Pendred syndrome

NCBI-Disease-Corpus-rezarta-All

Id	Subject	Object	Predicate	Lexical cue
T1	35-51	SpecificDisease	denotes	Pendred syndrome
T2	53-69	SpecificDisease	denotes	Pendred syndrome
T3	416-423	Modifier	denotes	Pendred
T4	894-901	Modifier	denotes	Pendred
T5	1190-1206	SpecificDisease	denotes	Pendred syndrome

NCBI-Disease-Corpus-4oGuideline-All

Id	Subject	Object	Predicate	Lexical cue
T1	35-51	SpecificDisease	denotes	Pendred syndrome
T2	53-69	SpecificDisease	denotes	Pendred syndrome
T3	76-104	DiseaseClass	denotes	autosomal recessive disorder
T4	1190-1206	SpecificDisease	denotes	Pendred syndrome

NCBI-Disease-Corpus-Simple-All

Id	Subject	Object	Predicate	Lexical cue
T1	35-51	SpecificDisease	denotes	Pendred syndrome
T2	53-69	SpecificDisease	denotes	Pendred syndrome
T3	138-146	SpecificDisease	denotes	deafness
T4	151-157	SpecificDisease	denotes	goiter
T5	416-423	SpecificDisease	denotes	Pendred
T6	894-901	SpecificDisease	denotes	Pendred
T7	1190-1206	SpecificDisease	denotes	Pendred syndrome

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Id	Subject	Object	Predicate	Lexical cue
T1	35-51	SpecificDisease	denotes	Pendred syndrome
T2	53-69	SpecificDisease	denotes	Pendred syndrome
T3	229-236	Modifier	denotes	disease
T4	416-423	Modifier	denotes	Pendred
T5	894-901	Modifier	denotes	Pendred
T6	1190-1206	SpecificDisease	denotes	Pendred syndrome

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Id	Subject	Object	Predicate	Lexical cue
T1	35-51	SpecificDisease	denotes	Pendred syndrome
T2	53-69	SpecificDisease	denotes	Pendred syndrome
T3	151-157	DiseaseClass	denotes	goiter
T4	416-423	Modifier	denotes	Pendred
T5	894-901	Modifier	denotes	Pendred
T6	1190-1206	SpecificDisease	denotes	Pendred syndrome