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PubMed:22988862 / 77-189 JSONTXT

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Inflammaging

Id Subject Object Predicate Lexical cue
T2 0-112 Sentence denotes Mutations in LRRK2 (leucine-rich repeat kinase 2) are the most common genetic cause of PD (Parkinson's disease).
T2 0-112 Sentence denotes Mutations in LRRK2 (leucine-rich repeat kinase 2) are the most common genetic cause of PD (Parkinson's disease).

c_corpus

Id Subject Object Predicate Lexical cue
T16 13-18 PR:Q5S006 denotes LRRK2
T17 13-18 PR:000003033 denotes LRRK2
T18 13-18 PR:Q5S007 denotes LRRK2
T20 20-27 6308 denotes leucine
T21 20-27 SO:0001437 denotes leucine
T19 20-27 CHEBI:15603 denotes leucine
T22 20-27 D007930 denotes leucine
T23 20-27 CHEBI:25017 denotes leucine
T24 20-27 D007930 denotes leucine
T25 33-39 SO:0001068 denotes repeat
T30 91-110 D010300 denotes Parkinson's disease
T31 91-110 D010300 denotes Parkinson's disease

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 91-100 HP_0001300 denotes Parkinson

Allie

Id Subject Object Predicate Lexical cue
SS1_22988862_1_0 20-48 expanded denotes leucine-rich repeat kinase 2
SS2_22988862_1_0 13-18 abbr denotes LRRK2
SS1_22988862_1_1 91-110 expanded denotes Parkinson's disease
SS2_22988862_1_1 87-89 abbr denotes PD
AE1_22988862_1_0 SS1_22988862_1_0 SS2_22988862_1_0 abbreviatedTo leucine-rich repeat kinase 2,LRRK2
AE1_22988862_1_1 SS1_22988862_1_1 SS2_22988862_1_1 abbreviatedTo Parkinson's disease,PD

UseCases_ArguminSci_Discourse

Id Subject Object Predicate Lexical cue
T2 0-112 DRI_Approach denotes Mutations in LRRK2 (leucine-rich repeat kinase 2) are the most common genetic cause of PD (Parkinson's disease).

PubMed_ArguminSci

Id Subject Object Predicate Lexical cue
T1 0-112 DRI_Approach denotes Mutations in LRRK2 (leucine-rich repeat kinase 2) are the most common genetic cause of PD (Parkinson's disease).