PubMed:21943124 / 544-696 JSON TXT

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Id	Subject	Object	Predicate	Lexical cue
TextSentencer_T6	0-152	Sentence	denotes	We present a child with Apert syndrome in whom routine genetic testing had excluded the FGFR2 missense mutations commonly associated with this disorder.
T6	0-152	Sentence	denotes	We present a child with Apert syndrome in whom routine genetic testing had excluded the FGFR2 missense mutations commonly associated with this disorder.

Id	Subject	Object	Predicate	Lexical cue
T2	88-93	gene:2263	denotes	FGFR2
T3	24-38	disease:C0001193	denotes	Apert syndrome
R2	T2	T3	associated_with	FGFR2,Apert syndrome

Id	Subject	Object	Predicate	Lexical cue
AB2	24-38	ORDO:87	denotes	Apert syndrome