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PubMed:23241745 / 126-248 JSONTXT

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c_corpus

Id Subject Object Predicate Lexical cue
T16 17-24 6308 denotes leucine
T17 17-24 SO:0001437 denotes leucine
T15 17-24 CHEBI:15603 denotes leucine
T18 17-24 D007930 denotes leucine
T19 17-24 CHEBI:25017 denotes leucine
T20 17-24 D007930 denotes leucine
T21 30-36 SO:0001068 denotes repeat
T22 47-52 PR:Q5S006 denotes LRRK2
T23 47-52 PR:000003033 denotes LRRK2
T24 47-52 PR:Q5S007 denotes LRRK2
T25 54-58 SO:0000704 denotes gene
T30 97-116 D010300 denotes Parkinson's disease
T31 97-116 D010300 denotes Parkinson's disease

Allie

Id Subject Object Predicate Lexical cue
SS1_23241745_1_0 17-45 expanded denotes leucine-rich repeat kinase 2
SS2_23241745_1_0 47-52 abbr denotes LRRK2
SS1_23241745_1_1 97-116 expanded denotes Parkinson's disease
SS2_23241745_1_1 118-120 abbr denotes PD
AE1_23241745_1_0 SS1_23241745_1_0 SS2_23241745_1_0 abbreviatedTo leucine-rich repeat kinase 2,LRRK2
AE1_23241745_1_1 SS1_23241745_1_1 SS2_23241745_1_1 abbreviatedTo Parkinson's disease,PD

UseCases_ArguminSci_Discourse

Id Subject Object Predicate Lexical cue
T2 0-122 DRI_Approach denotes Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene are the most common cause of familial Parkinson's disease (PD).

PubMed_ArguminSci

Id Subject Object Predicate Lexical cue
T1 0-122 DRI_Approach denotes Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene are the most common cause of familial Parkinson's disease (PD).

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 97-106 HP_0001300 denotes Parkinson