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PubMed:18258746 / 50-196 JSONTXT

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c_corpus

Id Subject Object Predicate Lexical cue
T17 17-24 6308 denotes leucine
T18 17-24 SO:0001437 denotes leucine
T16 17-24 CHEBI:15603 denotes leucine
T19 17-24 D007930 denotes leucine
T20 17-24 CHEBI:25017 denotes leucine
T21 17-24 D007930 denotes leucine
T22 30-36 SO:0001068 denotes repeat
T23 45-50 PR:Q5S006 denotes LRRK2
T24 45-50 PR:000003033 denotes LRRK2
T25 45-50 PR:Q5S007 denotes LRRK2
T26 52-56 SO:0000704 denotes gene
T27 63-73 D000067562 denotes late-onset
T28 63-73 D000067562 denotes late-onset
T29 74-92 C566739 denotes autosomal dominant
T34 93-112 D010300 denotes Parkinson's disease
T35 93-112 D010300 denotes Parkinson's disease

PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 25-29 DiseaseOrPhenotypicFeature denotes rich 0015404
T2 74-112 DiseaseOrPhenotypicFeature denotes autosomal dominant Parkinson's disease 0011220
T3 114-116 DiseaseOrPhenotypicFeature denotes PD 0008199|0015873|0005180

UseCases_ArguminSci_Discourse

Id Subject Object Predicate Lexical cue
T2 0-146 DRI_Challenge denotes Mutations in the leucine-rich repeat kinase (LRRK2) gene cause late-onset autosomal dominant Parkinson's disease (PD) with pleiomorphic pathology.

PubMed_ArguminSci

Id Subject Object Predicate Lexical cue
T1 0-146 DRI_Approach denotes Mutations in the leucine-rich repeat kinase (LRRK2) gene cause late-onset autosomal dominant Parkinson's disease (PD) with pleiomorphic pathology.