> top > docs > PubMed:21972245 > spans > 161-341 > annotations

PubMed:21972245 / 161-341 JSONTXT

Annnotations TAB JSON ListView MergeView

c_corpus

Id Subject Object Predicate Lexical cue
T18 17-24 6308 denotes leucine
T19 17-24 SO:0001437 denotes leucine
T17 17-24 CHEBI:15603 denotes leucine
T20 17-24 D007930 denotes leucine
T21 17-24 CHEBI:25017 denotes leucine
T22 17-24 D007930 denotes leucine
T23 30-36 SO:0001068 denotes repeat
T24 46-50 SO:0000704 denotes gene
T25 52-57 PR:Q5S006 denotes LRRK2
T26 52-57 PR:000003033 denotes LRRK2
T27 52-57 PR:Q5S007 denotes LRRK2
T32 96-115 D010300 denotes Parkinson's disease
T33 96-115 D010300 denotes Parkinson's disease
T36 136-154 C566739 denotes autosomal dominant

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 96-105 HP_0001300 denotes Parkinson
T2 136-154 HP_0000006 denotes autosomal dominant

Allie

Id Subject Object Predicate Lexical cue
SS1_21972245_1_0 17-50 expanded denotes leucine-rich repeat kinase 2 gene
SS2_21972245_1_0 52-57 abbr denotes LRRK2
SS1_21972245_1_1 96-115 expanded denotes Parkinson's disease
SS2_21972245_1_1 117-119 abbr denotes PD
AE1_21972245_1_0 SS1_21972245_1_0 SS2_21972245_1_0 abbreviatedTo leucine-rich repeat kinase 2 gene,LRRK2
AE1_21972245_1_1 SS1_21972245_1_1 SS2_21972245_1_1 abbreviatedTo Parkinson's disease,PD

UseCases_ArguminSci_Discourse

Id Subject Object Predicate Lexical cue
T2 0-180 DRI_Approach denotes Mutations in the leucine-rich repeat kinase 2 gene (LRRK2) are the most common genetic cause of Parkinson's disease (PD) and cause both autosomal dominant familial and sporadic PD.

PubMed_ArguminSci

Id Subject Object Predicate Lexical cue
T1 0-180 DRI_Approach denotes Mutations in the leucine-rich repeat kinase 2 gene (LRRK2) are the most common genetic cause of Parkinson's disease (PD) and cause both autosomal dominant familial and sporadic PD.