PMC:1189074 / 2951-3030 JSON TXT

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Id	Subject	Object	Predicate	Lexical cue
T531	0-79	sentence	denotes	Inherited MCAD deficiency exists in humans as an autosomal recessive disorder.
T532	1-10	VBN	denotes	Inherited
T533	16-26	NN	denotes	deficiency
T534	11-15	NN	denotes	MCAD
T535	27-33	VBZ	denotes	exists
T536	34-36	IN	denotes	in
T537	37-43	NNS	denotes	humans
T538	44-46	IN	denotes	as
T539	47-49	DT	denotes	an
T540	70-78	NN	denotes	disorder
T541	50-59	JJ	denotes	autosomal
T542	60-69	JJ	denotes	recessive
T543	78-79	.	denotes	.
R326	T532	T533	amod	Inherited,deficiency
R327	T533	T535	nsubj	deficiency,exists
R328	T534	T533	compound	MCAD,deficiency
R329	T536	T535	prep	in,exists
R330	T537	T536	pobj	humans,in
R331	T538	T535	prep	as,exists
R332	T539	T540	det	an,disorder
R333	T540	T538	pobj	disorder,as
R334	T541	T540	amod	autosomal,disorder
R335	T542	T540	amod	recessive,disorder
R336	T543	T535	punct	.,exists

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

Id	Subject	Object	Predicate	Lexical cue
T824	37-43	NCBITaxon:9606	denotes	humans
T825	50-59	GO:0030849	denotes	autosomal

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

Id	Subject	Object	Predicate	Lexical cue
T881	11-15	GO_PR_EXT:medium_chain_acyl_CoA_dehydrogenase	denotes	MCAD
T882	37-43	NCBITaxon:9606	denotes	humans
T883	50-59	GO:0030849	denotes	autosomal