PubMed:26744328 / 93-275 JSON TXT

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Id	Subject	Object	Predicate	Lexical cue
T16	13-20	6308	denotes	leucine
T17	13-20	SO:0001437	denotes	leucine
T15	13-20	CHEBI:15603	denotes	leucine
T18	13-20	D007930	denotes	leucine
T19	13-20	CHEBI:25017	denotes	leucine
T20	13-20	D007930	denotes	leucine
T21	26-32	SO:0001068	denotes	repeat
T22	43-48	PR:Q5S006	denotes	LRRK2
T23	43-48	PR:000003033	denotes	LRRK2
T24	43-48	PR:Q5S007	denotes	LRRK2
T26	56-87	D020734	denotes	autosomal-dominant Parkinsonism
T27	56-87	D020734	denotes	autosomal-dominant Parkinsonism
T34	148-155	SO:0000104	denotes	protein
T33	148-155	PR:000000001	denotes	protein
T30	148-155	GO:0003675	denotes	protein
T31	148-155	CHEBI:36080	denotes	protein
T32	148-155	CHEBI:11122	denotes	protein

Id	Subject	Object	Predicate	Lexical cue
T1	0-182	DRI_Outcome	denotes	Mutations in leucine-rich repeat kinase 2 (LRRK2) cause autosomal-dominant Parkinsonism with pleomorphic pathology including deposits of aggregated protein and neuronal degeneration.

Id	Subject	Object	Predicate	Lexical cue
26744328-1#13#41#gene120892	13-41	gene120892	denotes	leucine-rich repeat kinase 2
26744328-1#43#48#gene120892	43-48	gene120892	denotes	LRRK2
26744328-1#56#87#diseaseC0752098	56-87	diseaseC0752098	denotes	autosomal-dominant Parkinsonism
13#41#gene12089256#87#diseaseC0752098	26744328-1#13#41#gene120892	26744328-1#56#87#diseaseC0752098	associated_with	leucine-rich repeat kinase 2,autosomal-dominant Parkinsonism
43#48#gene12089256#87#diseaseC0752098	26744328-1#43#48#gene120892	26744328-1#56#87#diseaseC0752098	associated_with	LRRK2,autosomal-dominant Parkinsonism