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PubMed:26808467 / 141-282 JSONTXT

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c_corpus

Id Subject Object Predicate Lexical cue
T31 13-20 6308 denotes leucine
T32 13-20 SO:0001437 denotes leucine
T30 13-20 CHEBI:15603 denotes leucine
T33 13-20 D007930 denotes leucine
T34 13-20 CHEBI:25017 denotes leucine
T35 13-20 D007930 denotes leucine
T36 26-32 SO:0001068 denotes repeat
T37 43-48 PR:Q5S006 denotes LRRK2
T38 43-48 PR:000003033 denotes LRRK2
T39 43-48 PR:Q5S007 denotes LRRK2
T40 80-90 D000067562 denotes late onset
T41 80-90 D000067562 denotes late onset
T42 91-109 C566739 denotes autosomal dominant
T45 118-135 D010300 denotes Parkinson disease
T46 118-135 D010300 denotes Parkinson disease

PubMed_ArguminSci

Id Subject Object Predicate Lexical cue
T1 0-141 DRI_Approach denotes Mutations in leucine-rich repeat kinase 2 (LRRK2) are the most common causes of late onset autosomal dominant form of Parkinson disease (PD).