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PubMed:313733 JSON TXT

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performance-test

Id	Subject	Object	Predicate	Lexical cue
PD-UBERON-AE-B_T1	391-396	http://purl.obolibrary.org/obo/UBERON_0001977	denotes	Serum

sentences

Id	Subject	Object	Predicate	Lexical cue
TextSentencer_T1	0-74	Sentence	denotes	Hereditary C2 deficiency associated with common variable immunodeficiency.
TextSentencer_T2	75-309	Sentence	denotes	Homozygous C2 deficiency in a 19-year-old boy was associated with variable immunodeficiency manifested by marked hypoimmunoglobulinemia and impaired antibody responses, normal circulating B lymphocytes, and subnormal T-cell functions.
TextSentencer_T3	310-390	Sentence	denotes	Neither antilymphocytic autoantibodies nor chromosomal abnormalities were found.
TextSentencer_T4	391-512	Sentence	denotes	Serum immunoglobulin levels were within normal limits in his parents and brother who were heterozygous for C2 deficiency.
TextSentencer_T5	513-618	Sentence	denotes	The patient's lymphocytes were homozygous at the HLA-D locus but expressed an antigen different from DW2.
T1	0-74	Sentence	denotes	Hereditary C2 deficiency associated with common variable immunodeficiency.
T2	75-309	Sentence	denotes	Homozygous C2 deficiency in a 19-year-old boy was associated with variable immunodeficiency manifested by marked hypoimmunoglobulinemia and impaired antibody responses, normal circulating B lymphocytes, and subnormal T-cell functions.
T3	310-390	Sentence	denotes	Neither antilymphocytic autoantibodies nor chromosomal abnormalities were found.
T4	391-512	Sentence	denotes	Serum immunoglobulin levels were within normal limits in his parents and brother who were heterozygous for C2 deficiency.
T5	513-618	Sentence	denotes	The patient's lymphocytes were homozygous at the HLA-D locus but expressed an antigen different from DW2.

PubCasesHPO

Id	Subject	Object	Predicate	Lexical cue
TI1	57-73	HP:0002721	denotes	immunodeficiency
AB1	150-166	HP:0002721	denotes	immunodeficiency

PubCasesORDO

Id	Subject	Object	Predicate	Lexical cue
TI1	41-73	ORDO:1572	denotes	common variable immunodeficiency

NCBIDiseaseCorpus

Id	Subject	Object	Predicate	Lexical cue
T1	0-24	SpecificDisease:OMIM:217000	denotes	Hereditary C2 deficiency
T2	57-73	DiseaseClass:D007153	denotes	immunodeficiency
T3	86-99	SpecificDisease:OMIM:217000	denotes	C2 deficiency
T4	150-166	DiseaseClass:D007153	denotes	immunodeficiency
T5	188-210	DiseaseClass:D007153	denotes	hypoimmunoglobulinemia
T6	353-378	DiseaseClass:D002869	denotes	chromosomal abnormalities
T7	498-511	SpecificDisease:OMIM:217000	denotes	C2 deficiency

NCBI-Disease-Train

Id	Subject	Object	Predicate	Lexical cue	database_id
T4946	0-24	SpecificDisease	denotes	Hereditary C2 deficiency	OMIM:217000
T4947	57-73	DiseaseClass	denotes	immunodeficiency	D007153
T4948	86-99	SpecificDisease	denotes	C2 deficiency	OMIM:217000
T4949	150-166	DiseaseClass	denotes	immunodeficiency	D007153
T4950	188-210	DiseaseClass	denotes	hypoimmunoglobulinemia	D007153
T4951	353-378	DiseaseClass	denotes	chromosomal abnormalities	D002869
T4952	498-511	SpecificDisease	denotes	C2 deficiency	OMIM:217000

NCBI-Disease-Corpus-All

Id	Subject	Object	Predicate	Lexical cue	database_id
T4946	0-24	SpecificDisease	denotes	Hereditary C2 deficiency	OMIM:217000
T4947	57-73	DiseaseClass	denotes	immunodeficiency	D007153
T4948	86-99	SpecificDisease	denotes	C2 deficiency	OMIM:217000
T4949	150-166	DiseaseClass	denotes	immunodeficiency	D007153
T4950	188-210	DiseaseClass	denotes	hypoimmunoglobulinemia	D007153
T4951	353-378	DiseaseClass	denotes	chromosomal abnormalities	D002869
T4952	498-511	SpecificDisease	denotes	C2 deficiency	OMIM:217000

NCBI-Disease-Corpus-2stage-All

Id	Subject	Object	Predicate	Lexical cue
T1	11-24	SpecificDisease	denotes	C2 deficiency
T2	57-73	DiseaseClass	denotes	immunodeficiency
T3	86-99	SpecificDisease	denotes	C2 deficiency
T4	150-166	DiseaseClass	denotes	immunodeficiency
T5	498-511	SpecificDisease	denotes	C2 deficiency

NCBI-Disease-Corpus-rezarta-All

Id	Subject	Object	Predicate	Lexical cue
T1	11-24	SpecificDisease	denotes	C2 deficiency
T2	41-73	DiseaseClass	denotes	common variable immunodeficiency
T3	86-99	SpecificDisease	denotes	C2 deficiency
T4	141-166	DiseaseClass	denotes	variable immunodeficiency
T5	498-511	SpecificDisease	denotes	C2 deficiency

NCBI-Disease-Corpus-4oGuideline-All

Id	Subject	Object	Predicate	Lexical cue
T1	11-24	SpecificDisease	denotes	C2 deficiency
T2	41-73	DiseaseClass	denotes	common variable immunodeficiency
T3	86-99	SpecificDisease	denotes	C2 deficiency
T4	141-166	DiseaseClass	denotes	variable immunodeficiency
T5	498-511	SpecificDisease	denotes	C2 deficiency

NCBI-Disease-Corpus-Simple-All

Id	Subject	Object	Predicate	Lexical cue
T1	11-24	SpecificDisease	denotes	C2 deficiency
T2	41-73	SpecificDisease	denotes	common variable immunodeficiency
T3	86-99	SpecificDisease	denotes	C2 deficiency
T4	141-166	SpecificDisease	denotes	variable immunodeficiency
T5	188-210	Modifier	denotes	hypoimmunoglobulinemia
T6	282-291	Modifier	denotes	subnormal
T7	498-511	SpecificDisease	denotes	C2 deficiency