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PubMed:9848786 JSON TXT

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NCBI-Disease-Corpus-GPT5-withguidelines

Id	Subject	Object	Predicate	Lexical cue
T1	6-36	SpecificDisease	denotes	complement factor H deficiency
T2	53-78	SpecificDisease	denotes	hemolytic uremic syndrome
T3	210-223	DiseaseClass	denotes	renal disease
T4	285-321	SpecificDisease	denotes	idiopathic hemolytic uremic syndrome
T5	323-326	SpecificDisease	denotes	HUS
T6	891-910	SpecificDisease	denotes	Factor H deficiency
T7	923-944	DiseaseClass	denotes	complement deficiency
T8	961-964	SpecificDisease	denotes	HUS
T9	1050-1064	SpecificDisease	denotes	idiopathic HUS

NCBI-Disease-Corpus-GPT5-noguidelines

Id	Subject	Object	Predicate	Lexical cue
T1	0-36	SpecificDisease	denotes	Human complement factor H deficiency
T2	53-78	SpecificDisease	denotes	hemolytic uremic syndrome
T3	204-223	DiseaseClass	denotes	acute renal disease
T4	285-295	Modifier	denotes	idiopathic
T5	323-326	SpecificDisease	denotes	HUS
T6	361-371	Modifier	denotes	homozygous
T7	627-637	Modifier	denotes	homozygous
T8	791-803	Modifier	denotes	heterozygous
T9	891-910	SpecificDisease	denotes	Factor H deficiency
T10	923-944	DiseaseClass	denotes	complement deficiency
T11	961-964	SpecificDisease	denotes	HUS
T12	1050-1060	Modifier	denotes	idiopathic
T13	1061-1064	SpecificDisease	denotes	HUS

NCBI-Disease-Corpus-GPT5-guidelineprompt

Id	Subject	Object	Predicate	Lexical cue
T1	6-36	SpecificDisease	denotes	complement factor H deficiency
T2	53-78	SpecificDisease	denotes	hemolytic uremic syndrome
T3	204-223	DiseaseClass	denotes	acute renal disease
T4	285-321	SpecificDisease	denotes	idiopathic hemolytic uremic syndrome
T5	323-326	SpecificDisease	denotes	HUS
T6	891-910	SpecificDisease	denotes	Factor H deficiency
T7	923-944	DiseaseClass	denotes	complement deficiency
T8	961-964	SpecificDisease	denotes	HUS
T9	1050-1064	SpecificDisease	denotes	idiopathic HUS

NCBI-Disease-Corpus-Moderated1

Id	Subject	Object	Predicate	Lexical cue
T1	6-36	SpecificDisease	denotes	complement factor H deficiency
T2	53-78	SpecificDisease	denotes	hemolytic uremic syndrome
T3	210-223	DiseaseClass	denotes	renal disease
T4	285-321	SpecificDisease	denotes	idiopathic hemolytic uremic syndrome
T5	323-326	SpecificDisease	denotes	HUS
T6	891-910	SpecificDisease	denotes	Factor H deficiency
T7	923-944	DiseaseClass	denotes	complement deficiency
T8	961-964	SpecificDisease	denotes	HUS
T9	1050-1064	SpecificDisease	denotes	idiopathic HUS

DisGeNET

Id	Subject	Object	Predicate	Lexical cue
T0	1004-1006	gene:3075	denotes	FH
T1	1061-1064	disease:C0302810	denotes	HUS
T2	1014-1016	gene:3075	denotes	FH
T3	1061-1064	disease:C0302810	denotes	HUS
R1	T0	T1	associated_with	FH,HUS
R2	T2	T3	associated_with	FH,HUS

DisGeNET5_gene_disease

Id	Subject	Object	Predicate	Lexical cue
9848786-1#89#97#gene3075	169-177	gene3075	denotes	Factor H
9848786-1#99#101#gene3075	179-181	gene3075	denotes	FH
9848786-1#124#143#diseaseC1408247	204-223	diseaseC1408247	denotes	acute renal disease
9848786-7#38#40#gene3075	1004-1006	gene3075	denotes	FH
9848786-7#48#50#gene3075	1014-1016	gene3075	denotes	FH
9848786-7#95#98#diseaseC0019061	1061-1064	diseaseC0019061	denotes	HUS
89#97#gene3075124#143#diseaseC1408247	9848786-1#89#97#gene3075	9848786-1#124#143#diseaseC1408247	associated_with	Factor H,acute renal disease
99#101#gene3075124#143#diseaseC1408247	9848786-1#99#101#gene3075	9848786-1#124#143#diseaseC1408247	associated_with	FH,acute renal disease
38#40#gene307595#98#diseaseC0019061	9848786-7#38#40#gene3075	9848786-7#95#98#diseaseC0019061	associated_with	FH,HUS
48#50#gene307595#98#diseaseC0019061	9848786-7#48#50#gene3075	9848786-7#95#98#diseaseC0019061	associated_with	FH,HUS

PubCasesHPO

Id	Subject	Object	Predicate	Lexical cue
TI1	53-78	HP:0005575	denotes	hemolytic uremic syndrome
AB1	296-321	HP:0005575	denotes	hemolytic uremic syndrome
AB2	923-944	HP:0004431	denotes	complement deficiency

NCBIDiseaseCorpus

Id	Subject	Object	Predicate	Lexical cue
T1	0-36	SpecificDisease:OMIM:609814	denotes	Human complement factor H deficiency
T2	53-78	SpecificDisease:D006463	denotes	hemolytic uremic syndrome
T3	115-177	SpecificDisease:OMIM:609814	denotes	deficiency in the human complement regulatory protein Factor H
T4	204-223	SpecificDisease:D007674	denotes	acute renal disease
T5	296-321	SpecificDisease:D006463	denotes	hemolytic uremic syndrome
T6	323-326	SpecificDisease:D006463	denotes	HUS
T7	891-910	SpecificDisease:OMIM:609814	denotes	Factor H deficiency
T8	923-944	DiseaseClass:D007153	denotes	complement deficiency
T9	961-964	SpecificDisease:D006463	denotes	HUS
T10	1061-1064	SpecificDisease:D006463	denotes	HUS

NCBI-Disease-Test

Id	Subject	Object	Predicate	Lexical cue	database_id
T649	0-36	SpecificDisease	denotes	Human complement factor H deficiency	OMIM:609814
T650	53-78	SpecificDisease	denotes	hemolytic uremic syndrome	D006463
T651	115-177	SpecificDisease	denotes	deficiency in the human complement regulatory protein Factor H	OMIM:609814
T652	204-223	SpecificDisease	denotes	acute renal disease	D007674
T653	296-321	SpecificDisease	denotes	hemolytic uremic syndrome	D006463
T654	323-326	SpecificDisease	denotes	HUS	D006463
T655	891-910	SpecificDisease	denotes	Factor H deficiency	OMIM:609814
T656	923-944	DiseaseClass	denotes	complement deficiency	D007153
T657	961-964	SpecificDisease	denotes	HUS	D006463
T658	1061-1064	SpecificDisease	denotes	HUS	D006463

NCBI-Disease-Test-Assistant-Knowledge

Id	Subject	Object	Predicate	Lexical cue
T1	53-78	DiseaseClass	denotes	hemolytic uremic syndrome
T2	204-223	DiseaseClass	denotes	acute renal disease
T3	285-327	SpecificDisease	denotes	idiopathic hemolytic uremic syndrome (HUS)
T4	961-964	SpecificDisease	denotes	HUS
T5	1050-1064	SpecificDisease	denotes	idiopathic HUS

NCBI-Disease-Test-4o-NoGuidelineInPrompt

Id	Subject	Object	Predicate	Lexical cue
T1	53-78	SpecificDisease	denotes	hemolytic uremic syndrome
T2	204-223	DiseaseClass	denotes	acute renal disease
T3	285-327	SpecificDisease	denotes	idiopathic hemolytic uremic syndrome (HUS)
T4	361-371	Modifier	denotes	homozygous
T5	627-637	Modifier	denotes	homozygous
T6	791-803	Modifier	denotes	heterozygous
T7	961-964	SpecificDisease	denotes	HUS
T8	1050-1064	SpecificDisease	denotes	idiopathic HUS

NCBI-Disease-Corpus-o3-2

Id	Subject	Object	Predicate	Lexical cue
T1	0-36	SpecificDisease	denotes	Human complement factor H deficiency
T2	53-78	SpecificDisease	denotes	hemolytic uremic syndrome
T3	285-321	SpecificDisease	denotes	idiopathic hemolytic uremic syndrome
T4	323-326	SpecificDisease	denotes	HUS
T5	891-910	SpecificDisease	denotes	Factor H deficiency
T6	961-964	SpecificDisease	denotes	HUS
T7	1050-1064	SpecificDisease	denotes	idiopathic HUS

NCBI-Disease-Corpus-high-o3-1

Id	Subject	Object	Predicate	Lexical cue
T1	0-36	SpecificDisease	denotes	Human complement factor H deficiency
T2	53-78	SpecificDisease	denotes	hemolytic uremic syndrome
T3	204-223	DiseaseClass	denotes	acute renal disease
T4	285-321	SpecificDisease	denotes	idiopathic hemolytic uremic syndrome
T5	323-326	SpecificDisease	denotes	HUS
T6	891-910	SpecificDisease	denotes	Factor H deficiency
T7	961-964	SpecificDisease	denotes	HUS
T8	1050-1064	SpecificDisease	denotes	idiopathic HUS

NCBI-Disease-Corpus-high-o3-2

Id	Subject	Object	Predicate	Lexical cue
T1	0-36	SpecificDisease	denotes	Human complement factor H deficiency
T2	53-78	SpecificDisease	denotes	hemolytic uremic syndrome
T3	204-223	DiseaseClass	denotes	acute renal disease
T4	285-321	SpecificDisease	denotes	idiopathic hemolytic uremic syndrome
T5	323-326	SpecificDisease	denotes	HUS
T6	891-910	SpecificDisease	denotes	Factor H deficiency
T7	961-964	SpecificDisease	denotes	HUS
T8	1050-1064	SpecificDisease	denotes	idiopathic HUS

NCBI-Disease-Test-4o-GuidelineInPrompt

Id	Subject	Object	Predicate	Lexical cue
T1	53-78	SpecificDisease	denotes	hemolytic uremic syndrome
T2	204-223	DiseaseClass	denotes	acute renal disease
T3	285-321	SpecificDisease	denotes	idiopathic hemolytic uremic syndrome
T4	961-964	SpecificDisease	denotes	HUS
T5	1050-1064	SpecificDisease	denotes	idiopathic HUS

NCBI-Disease-Corpus-UpdatedGuideline

Id	Subject	Object	Predicate	Lexical cue
T1	53-78	SpecificDisease	denotes	hemolytic uremic syndrome
T2	115-125	DiseaseClass	denotes	deficiency
T3	169-182	SpecificDisease	denotes	Factor H (FH)
T4	204-215	Modifier	denotes	acute renal
T5	285-327	SpecificDisease	denotes	idiopathic hemolytic uremic syndrome (HUS)
T6	361-371	Modifier	denotes	homozygous
T7	434-442	SpecificDisease	denotes	Factor H
T8	495-508	Modifier	denotes	Factor H-like
T9	537-547	Modifier	denotes	FH-related
T10	627-637	Modifier	denotes	homozygous
T11	699-701	SpecificDisease	denotes	FH
T12	740-750	DiseaseClass	denotes	deficiency
T13	791-803	Modifier	denotes	heterozygous
T14	880-882	Modifier	denotes	FH
T15	891-910	SpecificDisease	denotes	Factor H deficiency
T16	961-964	SpecificDisease	denotes	HUS
T17	1004-1006	SpecificDisease	denotes	FH
T18	1014-1016	Modifier	denotes	FH
T19	1050-1064	SpecificDisease	denotes	idiopathic HUS

NCBI-Disease-Corpus-humanintheloop

Id	Subject	Object	Predicate	Lexical cue
T1	53-78	SpecificDisease	denotes	hemolytic uremic syndrome
T2	296-321	SpecificDisease	denotes	hemolytic uremic syndrome
T3	323-326	SpecificDisease	denotes	HUS
T4	961-964	SpecificDisease	denotes	HUS
T5	1061-1064	SpecificDisease	denotes	HUS

NCBI-Disease-Corpus-rezarta1

Id	Subject	Object	Predicate	Lexical cue
T1	53-78	SpecificDisease	denotes	hemolytic uremic syndrome
T2	169-910	Modifier	denotes	Factor H (FH) in the context of an acute renal disease. Five of the cases were observed in children presenting with idiopathic hemolytic uremic syndrome (HUS). Two of the children exhibited a homozygous deficiency characterized by the absence of the 150-kD form of Factor H and the presence, upon immunoblotting, of the 42-kD Factor H-like protein 1 (FHL-1) and other FH-related protein (FHR) bands. Southern blot and PCR analysis of DNA of one patient with homozygous deficiency ruled out the presence of a large deletion of the FH gene as the underlying defect for the deficiency. The other four children presented with heterozygous deficiency and exhibited a normal immunoblotting pattern of proteins of the FH family. Factor H deficiency
T3	177-190	DiseaseClass	denotes	(FH) in the
T4	263-288	SpecificDisease	denotes	ldren presenting with idi
T5	290-293	SpecificDisease	denotes	ath
T6	401-420	Modifier	denotes	he absence of the 1
T7	677-690	Modifier	denotes	large deletio
T8	869-882	Modifier	denotes	ins of the FH
T9	891-910	SpecificDisease	denotes	Factor H deficiency
T10	961-964	SpecificDisease	denotes	HUS
T11	1004-1006	SpecificDisease	denotes	FH
T12	1061-1064	SpecificDisease	denotes	HUS

NCBI-Disease-Corpus-All

Id	Subject	Object	Predicate	Lexical cue	database_id
T649	0-36	SpecificDisease	denotes	Human complement factor H deficiency	OMIM:609814
T650	53-78	SpecificDisease	denotes	hemolytic uremic syndrome	D006463
T651	115-177	SpecificDisease	denotes	deficiency in the human complement regulatory protein Factor H	OMIM:609814
T652	204-223	SpecificDisease	denotes	acute renal disease	D007674
T653	296-321	SpecificDisease	denotes	hemolytic uremic syndrome	D006463
T654	323-326	SpecificDisease	denotes	HUS	D006463
T655	891-910	SpecificDisease	denotes	Factor H deficiency	OMIM:609814
T656	923-944	DiseaseClass	denotes	complement deficiency	D007153
T657	961-964	SpecificDisease	denotes	HUS	D006463
T658	1061-1064	SpecificDisease	denotes	HUS	D006463

NCBI-Disease-Corpus-2stage-All

Id	Subject	Object	Predicate	Lexical cue
T1	53-78	SpecificDisease	denotes	hemolytic uremic syndrome
T2	296-321	SpecificDisease	denotes	hemolytic uremic syndrome
T3	323-326	SpecificDisease	denotes	HUS
T4	961-964	SpecificDisease	denotes	HUS
T5	1061-1064	SpecificDisease	denotes	HUS

NCBI-Disease-Corpus-rezarta-All

Id	Subject	Object	Predicate	Lexical cue
T1	53-78	SpecificDisease	denotes	hemolytic uremic syndrome
T2	285-321	SpecificDisease	denotes	idiopathic hemolytic uremic syndrome
T3	323-326	SpecificDisease	denotes	HUS
T4	891-910	SpecificDisease	denotes	Factor H deficiency
T5	961-964	SpecificDisease	denotes	HUS
T6	1050-1064	SpecificDisease	denotes	idiopathic HUS

NCBI-Disease-Corpus-4oGuideline-All

Id	Subject	Object	Predicate	Lexical cue
T1	53-78	SpecificDisease	denotes	hemolytic uremic syndrome
T2	210-223	DiseaseClass	denotes	renal disease
T3	285-321	SpecificDisease	denotes	idiopathic hemolytic uremic syndrome
T4	961-964	SpecificDisease	denotes	HUS
T5	1050-1064	SpecificDisease	denotes	idiopathic HUS

NCBI-Disease-Corpus-Simple-All

Id	Subject	Object	Predicate	Lexical cue
T1	0-36	SpecificDisease	denotes	Human complement factor H deficiency
T2	53-78	DiseaseClass	denotes	hemolytic uremic syndrome
T3	204-209	Modifier	denotes	acute
T4	210-223	DiseaseClass	denotes	renal disease
T5	285-327	SpecificDisease	denotes	idiopathic hemolytic uremic syndrome (HUS)
T6	361-371	Modifier	denotes	homozygous
T7	627-637	Modifier	denotes	homozygous
T8	791-803	Modifier	denotes	heterozygous
T9	961-964	SpecificDisease	denotes	HUS
T10	1050-1064	SpecificDisease	denotes	idiopathic HUS

123456

Id	Subject	Object	Predicate	Lexical cue
T1	53-78	SpecificDisease	denotes	hemolytic uremic syndrome
T2	296-321	SpecificDisease	denotes	hemolytic uremic syndrome
T3	323-326	SpecificDisease	denotes	HUS
T4	961-964	SpecificDisease	denotes	HUS
T5	1061-1064	SpecificDisease	denotes	HUS

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Id	Subject	Object	Predicate	Lexical cue
T1	53-78	SpecificDisease	denotes	hemolytic uremic syndrome
T2	115-125	Modifier	denotes	deficiency
T3	296-321	SpecificDisease	denotes	hemolytic uremic syndrome
T4	323-326	SpecificDisease	denotes	HUS
T5	372-382	Modifier	denotes	deficiency
T6	638-648	Modifier	denotes	deficiency
T7	740-750	Modifier	denotes	deficiency
T8	804-814	Modifier	denotes	deficiency
T9	891-910	SpecificDisease	denotes	Factor H deficiency
T10	934-944	Modifier	denotes	deficiency
T11	961-964	SpecificDisease	denotes	HUS
T12	1061-1064	SpecificDisease	denotes	HUS