PubMed:10072068 JSON TXT

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Id	Subject	Object	Predicate	Lexical cue
T1	0-5	DNA	denotes	RFX-B
T2	92-104	protein	denotes	MHC class II
T3	193-205	protein	denotes	MHC class II
T4	382-415	protein	denotes	MHC class II transcription factor
T5	416-419	protein	denotes	RFX
T6	442-453	protein	denotes	RFX complex
T7	556-561	DNA	denotes	RFX-B
T8	563-568	DNA	denotes	RFX-B
T9	597-622	protein	denotes	BLS complementation group
T10	624-631	protein	denotes	group B
T11	663-673	cell_line	denotes	cell lines
T12	720-738	protein	denotes	DNA-binding domain

Id	Subject	Object	Predicate	Lexical cue
10072068-0#0#5#gene8625	0-5	gene8625	denotes	RFX-B
10072068-0#63#87#diseaseC0242583	63-87	diseaseC0242583	denotes	bare lymphocyte syndrome
10072068-0#63#87#diseaseC2931418	63-87	diseaseC2931418	denotes	bare lymphocyte syndrome
10072068-1#70#73#gene3107	193-196	gene3107	denotes	MHC
10072068-1#4#28#diseaseC2931418	127-151	diseaseC2931418	denotes	bare lymphocyte syndrome
10072068-1#30#33#diseaseC2931418	153-156	diseaseC2931418	denotes	BLS
0#5#gene862563#87#diseaseC0242583	10072068-0#0#5#gene8625	10072068-0#63#87#diseaseC0242583	associated_with	RFX-B,bare lymphocyte syndrome
0#5#gene862563#87#diseaseC2931418	10072068-0#0#5#gene8625	10072068-0#63#87#diseaseC2931418	associated_with	RFX-B,bare lymphocyte syndrome
70#73#gene31074#28#diseaseC2931418	10072068-1#70#73#gene3107	10072068-1#4#28#diseaseC2931418	associated_with	MHC,bare lymphocyte syndrome
70#73#gene310730#33#diseaseC2931418	10072068-1#70#73#gene3107	10072068-1#30#33#diseaseC2931418	associated_with	MHC,BLS

Id	Subject	Object	Predicate	Lexical cue
C1	0-5	NP	denotes	RFX-B
C2	59-87	NP	denotes	the bare lymphocyte syndrome
C3	89-121	NP	denotes	an MHC class II immunodeficiency
C4	123-157	NP	denotes	The bare lymphocyte syndrome (BLS)
C5	438-453	NP	denotes	the RFX complex
C6	468-471	NP	denotes	its
C7	535-547	NP	denotes	a novel gene
C8	556-561	NP	denotes	RFX-B
C9	563-568	NP	denotes	RFX-B
C10	581-632	NP	denotes	the predominant BLS complementation group (group B)
C11	679-693	NP	denotes	this BLS group
C12	756-777	NP	denotes	three ankyrin repeats
C13	778-782	NP	denotes	that
R1	C3	C2	coref-appos	an MHC class II immunodeficiency,the bare lymphocyte syndrome
R2	C4	C2	coref-ident	The bare lymphocyte syndrome (BLS),the bare lymphocyte syndrome
R3	C6	C5	coref-pron	its,the RFX complex
R4	C7	C1	coref-ident	a novel gene,RFX-B
R5	C8	C7	coref-ident	RFX-B,a novel gene
R6	C9	C8	coref-ident	RFX-B,RFX-B
R7	C11	C10	coref-ident	this BLS group,the predominant BLS complementation group (group B)
R8	C13	C12	coref-relat	that,three ankyrin repeats

Id	Subject	Object	Predicate	Lexical cue
S1	0-122	Sentence	denotes	RFX-B is the gene responsible for the most common cause of the bare lymphocyte syndrome, an MHC class II immunodeficiency.
S2	123-292	Sentence	denotes	The bare lymphocyte syndrome (BLS) is characterized by the absence of MHC class II transcription and humoral- and cellular-mediated immune responses to foreign antigens.
S3	293-420	Sentence	denotes	Three of the four BLS genetic complementation groups have defects in the activity of the MHC class II transcription factor RFX.
S4	421-487	Sentence	denotes	We have purified the RFX complex and sequenced its three subunits.
S5	488-562	Sentence	denotes	The sequence of the smallest subunit describes a novel gene, termed RFX-B.
S6	563-694	Sentence	denotes	RFX-B complements the predominant BLS complementation group (group B) and was found to be mutant in cell lines from this BLS group.
S7	695-842	Sentence	denotes	The protein has no known DNA-binding domain but does contain three ankyrin repeats that are likely to be important in protein-protein interactions.

Id	Subject	Object	Predicate	Lexical cue
T1	0-5	DNA_domain_or_region	denotes	RFX-B
T2	63-87	other_name	denotes	bare lymphocyte syndrome
T3	92-104	protein_family_or_group	denotes	MHC class II
T4	127-151	other_name	denotes	bare lymphocyte syndrome
T5	153-156	other_name	denotes	BLS
T6	193-205	protein_family_or_group	denotes	MHC class II
T7	311-314	other_name	denotes	BLS
T8	382-415	protein_family_or_group	denotes	MHC class II transcription factor
T9	416-419	protein_molecule	denotes	RFX
T10	442-445	protein_molecule	denotes	RFX
T11	556-561	DNA_domain_or_region	denotes	RFX-B
T12	563-568	DNA_domain_or_region	denotes	RFX-B
T13	597-600	other_name	denotes	BLS
T14	624-631	protein_family_or_group	denotes	group B
T15	663-673	cell_line	denotes	cell lines
T16	684-687	other_name	denotes	BLS
T17	720-738	protein_domain_or_region	denotes	DNA-binding domain
T18	813-841	other_name	denotes	protein-protein interactions

Id	Subject	Object	Predicate	Lexical cue
T0	563-568	gene:8625	denotes	RFX-B
T1	597-600	disease:C0242583	denotes	BLS
T2	563-568	gene:8625	denotes	RFX-B
T3	597-600	disease:C2931418	denotes	BLS
T4	563-568	gene:8625	denotes	RFX-B
T5	684-687	disease:C0242583	denotes	BLS
T6	563-568	gene:8625	denotes	RFX-B
T7	684-687	disease:C2931418	denotes	BLS
R1	T0	T1	associated_with	RFX-B,BLS
R2	T2	T3	associated_with	RFX-B,BLS
R3	T4	T5	associated_with	RFX-B,BLS
R4	T6	T7	associated_with	RFX-B,BLS