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PubMed:19545277 / 167-304 JSONTXT

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c_corpus

Id Subject Object Predicate Lexical cue
T17 32-39 6308 denotes leucine
T18 32-39 SO:0001437 denotes leucine
T16 32-39 CHEBI:15603 denotes leucine
T19 32-39 D007930 denotes leucine
T20 32-39 CHEBI:25017 denotes leucine
T21 32-39 D007930 denotes leucine
T22 45-51 SO:0001068 denotes repeat
T23 62-67 PR:Q5S006 denotes LRRK2
T24 62-67 PR:000003033 denotes LRRK2
T25 62-67 PR:Q5S007 denotes LRRK2
T26 106-116 D000067562 denotes late-onset
T27 106-116 D000067562 denotes late-onset
T32 117-136 D010300 denotes Parkinson's disease
T33 117-136 D010300 denotes Parkinson's disease

UseCases_ArguminSci_Discourse

Id Subject Object Predicate Lexical cue
T2 0-137 DRI_Background denotes Autosomal dominant mutations in leucine-rich repeat kinase 2 (LRRK2) are the most common genetic cause of late-onset Parkinson's disease.

PubMed_ArguminSci

Id Subject Object Predicate Lexical cue
T1 0-137 DRI_Background denotes Autosomal dominant mutations in leucine-rich repeat kinase 2 (LRRK2) are the most common genetic cause of late-onset Parkinson's disease.

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
19545277-1#32#60#gene120892 32-60 gene120892 denotes leucine-rich repeat kinase 2
19545277-1#62#67#gene120892 62-67 gene120892 denotes LRRK2
19545277-1#106#136#diseaseC3160718 106-136 diseaseC3160718 denotes late-onset Parkinson's disease
32#60#gene120892106#136#diseaseC3160718 19545277-1#32#60#gene120892 19545277-1#106#136#diseaseC3160718 associated_with leucine-rich repeat kinase 2,late-onset Parkinson's disease
62#67#gene120892106#136#diseaseC3160718 19545277-1#62#67#gene120892 19545277-1#106#136#diseaseC3160718 associated_with LRRK2,late-onset Parkinson's disease