> top > docs > PubMed:26744328 > spans > 0-182 > annotations

PubMed:26744328 / 0-182 JSONTXT

Annnotations TAB JSON ListView MergeView

c_corpus

Id Subject Object Predicate Lexical cue
T1 0-11 Q9Y6H5 denotes Synphilin-1
T2 0-11 PR:000015323 denotes Synphilin-1
T3 0-11 Q99ME3 denotes Synphilin-1
T4 30-35 PR:Q5S006 denotes LRRK2
T5 30-35 PR:000003033 denotes LRRK2
T6 30-35 PR:Q5S007 denotes LRRK2
T11 65-84 D010300 denotes Parkinson's disease
T12 65-84 D010300 denotes Parkinson's disease
T16 106-113 6308 denotes leucine
T17 106-113 SO:0001437 denotes leucine
T15 106-113 CHEBI:15603 denotes leucine
T18 106-113 D007930 denotes leucine
T19 106-113 CHEBI:25017 denotes leucine
T20 106-113 D007930 denotes leucine
T21 119-125 SO:0001068 denotes repeat
T22 136-141 PR:Q5S006 denotes LRRK2
T23 136-141 PR:000003033 denotes LRRK2
T24 136-141 PR:Q5S007 denotes LRRK2
T26 149-180 D020734 denotes autosomal-dominant Parkinsonism
T27 149-180 D020734 denotes autosomal-dominant Parkinsonism

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
26744328-0#0#11#gene9627 0-11 gene9627 denotes Synphilin-1
26744328-0#30#35#gene120892 30-35 gene120892 denotes LRRK2
26744328-0#65#84#diseaseC0030567 65-84 diseaseC0030567 denotes Parkinson's disease
26744328-1#13#41#gene120892 106-134 gene120892 denotes leucine-rich repeat kinase 2
26744328-1#43#48#gene120892 136-141 gene120892 denotes LRRK2
26744328-1#56#87#diseaseC0752098 149-180 diseaseC0752098 denotes autosomal-dominant Parkinsonism
0#11#gene962765#84#diseaseC0030567 26744328-0#0#11#gene9627 26744328-0#65#84#diseaseC0030567 associated_with Synphilin-1,Parkinson's disease
30#35#gene12089265#84#diseaseC0030567 26744328-0#30#35#gene120892 26744328-0#65#84#diseaseC0030567 associated_with LRRK2,Parkinson's disease
13#41#gene12089256#87#diseaseC0752098 26744328-1#13#41#gene120892 26744328-1#56#87#diseaseC0752098 associated_with leucine-rich repeat kinase 2,autosomal-dominant Parkinsonism
43#48#gene12089256#87#diseaseC0752098 26744328-1#43#48#gene120892 26744328-1#56#87#diseaseC0752098 associated_with LRRK2,autosomal-dominant Parkinsonism