PubMed:26744332 / 126-421 JSON TXT

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Id	Subject	Object	Predicate	Lexical cue
T25	13-20	6308	denotes	leucine
T26	13-20	SO:0001437	denotes	leucine
T24	13-20	CHEBI:15603	denotes	leucine
T27	13-20	D007930	denotes	leucine
T28	13-20	CHEBI:25017	denotes	leucine
T29	13-20	D007930	denotes	leucine
T30	26-32	SO:0001068	denotes	repeat
T31	43-48	PR:Q5S006	denotes	LRRK2
T32	43-48	PR:000003033	denotes	LRRK2
T33	43-48	PR:Q5S007	denotes	LRRK2
T34	58-68	D000067562	denotes	late-onset
T35	58-68	D000067562	denotes	late-onset
T36	70-88	C566739	denotes	autosomal dominant
T41	89-108	D010300	denotes	Parkinson's disease
T42	89-108	D010300	denotes	Parkinson's disease
T49	147-155	3628	denotes	dopamine
T45	147-155	CHEBI:59905	denotes	dopamine
T46	147-155	CHEBI:18243	denotes	dopamine
T47	147-155	D004298	denotes	dopamine
T48	147-155	D004298	denotes	dopamine
T51	171-201	UBERON:0001966	denotes	substantia nigra pars compacta
T52	171-201	UBERON:0001965	denotes	substantia nigra pars compacta
T53	188-192	PR:P07814	denotes	pars
T54	188-192	PR:000007144	denotes	pars
T60	216-224	3628	denotes	dopamine
T56	216-224	CHEBI:59905	denotes	dopamine
T57	216-224	CHEBI:18243	denotes	dopamine
T58	216-224	D004298	denotes	dopamine
T59	216-224	D004298	denotes	dopamine
T61	225-242	GO:0007268	denotes	neurotransmission

Id	Subject	Object	Predicate	Lexical cue
T1	0-295	DRI_Challenge	denotes	Mutations in leucine-rich repeat kinase 2 (LRRK2) lead to late-onset, autosomal dominant Parkinson's disease, characterized by the degeneration of dopamine neurons of the substantia nigra pars compacta, a deficit in dopamine neurotransmission and the development of motor and non-motor symptoms.

Id	Subject	Object	Predicate	Lexical cue
26744332-1#13#41#gene120892	13-41	gene120892	denotes	leucine-rich repeat kinase 2
26744332-1#43#48#gene120892	43-48	gene120892	denotes	LRRK2
26744332-1#280#294#diseaseC0426980	280-294	diseaseC0426980	denotes	motor symptoms
26744332-1#70#108#diseaseC3489791	70-108	diseaseC3489791	denotes	autosomal dominant Parkinson's disease
26744332-1#280#294#diseaseC0426980	280-294	diseaseC0426980	denotes	motor symptoms
13#41#gene120892280#294#diseaseC0426980	26744332-1#13#41#gene120892	26744332-1#280#294#diseaseC0426980	associated_with	leucine-rich repeat kinase 2,motor symptoms
13#41#gene12089270#108#diseaseC3489791	26744332-1#13#41#gene120892	26744332-1#70#108#diseaseC3489791	associated_with	leucine-rich repeat kinase 2,autosomal dominant Parkinson's disease
13#41#gene120892280#294#diseaseC0426980	26744332-1#13#41#gene120892	26744332-1#280#294#diseaseC0426980	associated_with	leucine-rich repeat kinase 2,motor symptoms
43#48#gene120892280#294#diseaseC0426980	26744332-1#43#48#gene120892	26744332-1#280#294#diseaseC0426980	associated_with	LRRK2,motor symptoms
43#48#gene12089270#108#diseaseC3489791	26744332-1#43#48#gene120892	26744332-1#70#108#diseaseC3489791	associated_with	LRRK2,autosomal dominant Parkinson's disease
43#48#gene120892280#294#diseaseC0426980	26744332-1#43#48#gene120892	26744332-1#280#294#diseaseC0426980	associated_with	LRRK2,motor symptoms