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NCBI-Disease-Corpus-GPT5-withguidelines

Id	Subject	Object	Predicate	Lexical cue
T1	35-53	Modifier	denotes	myotonic dystrophy
T2	319-337	SpecificDisease	denotes	myotonic dystrophy

NCBI-Disease-Corpus-GPT5-noguidelines

Id	Subject	Object	Predicate	Lexical cue
T1	17-34	Modifier	denotes	severely affected
T2	35-53	SpecificDisease	denotes	myotonic dystrophy
T3	319-337	SpecificDisease	denotes	myotonic dystrophy
T4	790-795	Modifier	denotes	young
T5	800-817	Modifier	denotes	severely affected
T6	962-969	DiseaseClass	denotes	disease
T7	974-984	Modifier	denotes	congenital

NCBI-Disease-Corpus-GPT5-guidelineprompt

Id	Subject	Object	Predicate	Lexical cue
T1	35-53	Modifier	denotes	myotonic dystrophy
T2	319-337	SpecificDisease	denotes	myotonic dystrophy

NCBI-Disease-Corpus-Moderated1

Id	Subject	Object	Predicate	Lexical cue
T1	35-53	Modifier	denotes	myotonic dystrophy
T2	319-337	SpecificDisease	denotes	myotonic dystrophy

DisGeNET

Id	Subject	Object	Predicate	Lexical cue
T0	257-261	gene:1760	denotes	DMPK
T1	319-337	disease:C0027126	denotes	myotonic dystrophy
T2	257-261	gene:1760	denotes	DMPK
T3	319-337	disease:C0410226	denotes	myotonic dystrophy
R1	T0	T1	associated_with	DMPK,myotonic dystrophy
R2	T2	T3	associated_with	DMPK,myotonic dystrophy

DisGeNET5_gene_disease

Id	Subject	Object	Predicate	Lexical cue
9463318-0#4#8#gene1760	4-8	gene1760	denotes	DMPK
9463318-0#35#53#diseaseC0027126	35-53	diseaseC0027126	denotes	myotonic dystrophy
4#8#gene176035#53#diseaseC0027126	9463318-0#4#8#gene1760	9463318-0#35#53#diseaseC0027126	associated_with	DMPK,myotonic dystrophy

NCBIDiseaseCorpus

Id	Subject	Object	Predicate	Lexical cue
T1	35-53	Modifier:D009223	denotes	myotonic dystrophy
T2	319-337	SpecificDisease:D009223	denotes	myotonic dystrophy

NCBI-Disease-Test

Id	Subject	Object	Predicate	Lexical cue	database_id
T712	35-53	Modifier	denotes	myotonic dystrophy	D009223
T713	319-337	SpecificDisease	denotes	myotonic dystrophy	D009223

NCBI-Disease-Test-Assistant-Knowledge

Id	Subject	Object	Predicate	Lexical cue
T1	35-53	SpecificDisease	denotes	myotonic dystrophy
T2	319-337	SpecificDisease	denotes	myotonic dystrophy
T3	962-969	SpecificDisease	denotes	disease

NCBI-Disease-Test-4o-NoGuidelineInPrompt

Id	Subject	Object	Predicate	Lexical cue
T1	35-53	SpecificDisease	denotes	myotonic dystrophy
T2	319-337	SpecificDisease	denotes	myotonic dystrophy
T3	962-969	SpecificDisease	denotes	disease
T4	974-984	Modifier	denotes	congenital

NCBI-Disease-Corpus-o3-2

Id	Subject	Object	Predicate	Lexical cue
T1	35-53	Modifier	denotes	myotonic dystrophy
T2	319-337	Modifier	denotes	myotonic dystrophy

NCBI-Disease-Corpus-high-o3-1

Id	Subject	Object	Predicate	Lexical cue
T1	35-53	Modifier	denotes	myotonic dystrophy
T2	319-337	Modifier	denotes	myotonic dystrophy

NCBI-Disease-Corpus-high-o3-2

Id	Subject	Object	Predicate	Lexical cue
T1	35-53	SpecificDisease	denotes	myotonic dystrophy
T2	319-337	SpecificDisease	denotes	myotonic dystrophy

NCBI-Disease-Test-4o-GuidelineInPrompt

Id	Subject	Object	Predicate	Lexical cue
T1	4-53	SpecificDisease	denotes	DMPK gene of severely affected myotonic dystrophy
T2	257-337	SpecificDisease	denotes	DMPK gene of normal individuals and of patients affected with myotonic dystrophy
T3	962-969	SpecificDisease	denotes	disease
T4	1222-1231	SpecificDisease	denotes	DMPK gene

NCBI-Disease-Corpus-UpdatedGuideline

Id	Subject	Object	Predicate	Lexical cue
T1	35-53	SpecificDisease	denotes	myotonic dystrophy
T2	319-337	SpecificDisease	denotes	myotonic dystrophy
T3	962-969	SpecificDisease	denotes	disease

NCBI-Disease-Corpus-humanintheloop

Id	Subject	Object	Predicate	Lexical cue
T1	35-53	Modifier	denotes	myotonic dystrophy
T2	319-337	SpecificDisease	denotes	myotonic dystrophy
T3	974-984	Modifier	denotes	congenital

NCBI-Disease-Corpus-rezarta1

Id	Subject	Object	Predicate	Lexical cue
T1	35-53	Modifier	denotes	myotonic dystrophy
T2	319-337	SpecificDisease	denotes	myotonic dystrophy
T3	962-969	DiseaseClass	denotes	disease

NCBI-Disease-Corpus-All

Id	Subject	Object	Predicate	Lexical cue	database_id
T712	35-53	Modifier	denotes	myotonic dystrophy	D009223
T713	319-337	SpecificDisease	denotes	myotonic dystrophy	D009223

NCBI-Disease-Corpus-2stage-All

Id	Subject	Object	Predicate	Lexical cue
T1	35-53	SpecificDisease	denotes	myotonic dystrophy
T2	319-337	SpecificDisease	denotes	myotonic dystrophy
T3	974-984	DiseaseClass	denotes	congenital

NCBI-Disease-Corpus-rezarta-All

Id	Subject	Object	Predicate	Lexical cue
T1	35-53	Modifier	denotes	myotonic dystrophy
T2	319-337	SpecificDisease	denotes	myotonic dystrophy
T3	962-969	DiseaseClass	denotes	disease

NCBI-Disease-Corpus-4oGuideline-All

Id	Subject	Object	Predicate	Lexical cue
T1	35-53	SpecificDisease	denotes	myotonic dystrophy
T2	319-337	SpecificDisease	denotes	myotonic dystrophy
T3	962-969	Modifier	denotes	disease
T4	974-984	Modifier	denotes	congenital

NCBI-Disease-Corpus-Simple-All

Id	Subject	Object	Predicate	Lexical cue
T1	35-53	SpecificDisease	denotes	myotonic dystrophy
T2	319-337	SpecificDisease	denotes	myotonic dystrophy
T3	962-969	SpecificDisease	denotes	disease
T4	974-984	Modifier	denotes	congenital

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Id	Subject	Object	Predicate	Lexical cue
T1	35-53	Modifier	denotes	myotonic dystrophy
T2	319-337	SpecificDisease	denotes	myotonic dystrophy
T3	974-984	Modifier	denotes	congenital

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Id	Subject	Object	Predicate	Lexical cue
T1	35-53	Modifier	denotes	myotonic dystrophy
T2	319-337	Modifier	denotes	myotonic dystrophy
T3	962-969	SpecificDisease	denotes	disease