PMC:1564426 / 3875-3997 JSON TXT

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Below, discontinuous spans are shown in the chain model. You can change it to the bag model.

Id	Subject	Object	Predicate	Lexical cue
T2259	1-10	GO:0030849	denotes	Autosomal
T2260	29-38	SO_EXT:sequence_alteration_entity_or_process	denotes	mutations
T2261	42-45	PR_EXT:000004122	denotes	APC

Below, discontinuous spans are shown in the chain model. You can change it to the bag model.

Id	Subject	Object	Predicate	Lexical cue
T2110	1-10	GO:0030849	denotes	Autosomal
T2111	42-45	PR:000004122	denotes	APC

Id	Subject	Object	Predicate	Lexical cue
T2580	0-122	sentence	denotes	Autosomal dominant germline mutations in APC cause familial adenomatous polypois (FAP) and its variant, Gardner syndrome.
T2581	1-10	JJ	denotes	Autosomal
T2582	29-38	NNS	denotes	mutations
T2583	11-19	JJ	denotes	dominant
T2584	20-28	NN	denotes	germline
T2585	46-51	VBP	denotes	cause
T2586	39-41	IN	denotes	in
T2587	42-45	NN	denotes	APC
T2588	52-60	JJ	denotes	familial
T2589	73-81	NN	denotes	polypois
T2590	61-72	JJ	denotes	adenomatous
T2591	82-83	-LRB-	denotes	(
T2592	83-86	NN	denotes	FAP
T2593	86-87	-RRB-	denotes	)
T2594	88-91	CC	denotes	and
T2595	92-95	PRP$	denotes	its
T2596	96-103	NN	denotes	variant
T2597	103-105	,	denotes	,
T2598	105-112	NNP	denotes	Gardner
T2599	113-121	NN	denotes	syndrome
T2600	121-122	.	denotes	.
R501	T2581	T2582	amod	Autosomal,mutations
R506	T2582	T2585	nsubj	mutations,cause
R510	T2583	T2582	amod	dominant,mutations
R514	T2584	T2582	compound	germline,mutations
R518	T2586	T2582	prep	in,mutations
R519	T2587	T2586	pobj	APC,in
R522	T2588	T2589	amod	familial,polypois
R526	T2589	T2585	dobj	polypois,cause
R529	T2590	T2589	amod	adenomatous,polypois
R533	T2591	T2589	punct	(,polypois
R537	T2592	T2589	appos	FAP,polypois
R541	T2593	T2589	punct	),polypois
R545	T2594	T2589	cc	and,polypois
R552	T2595	T2596	poss	its,variant
R556	T2596	T2589	conj	variant,polypois
R560	T2597	T2596	punct	", ",variant
R565	T2598	T2599	compound	Gardner,syndrome
R568	T2599	T2596	appos	syndrome,variant
R570	T2600	T2585	punct	.,cause