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PubMed:16240353 JSONTXT

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DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
16240353-0#0#6#geners34637584 0-6 geners34637584 denotes G2019S
16240353-0#64#83#diseaseC0030567 64-83 diseaseC0030567 denotes Parkinson's disease
16240353-1#106#112#geners34637584 191-197 geners34637584 denotes G2019S
16240353-1#47#85#diseaseC3489791 132-170 diseaseC3489791 denotes autosomal dominant Parkinson's disease
0#6#geners3463758464#83#diseaseC0030567 16240353-0#0#6#geners34637584 16240353-0#64#83#diseaseC0030567 associated_with G2019S,Parkinson's disease
106#112#geners3463758447#85#diseaseC3489791 16240353-1#106#112#geners34637584 16240353-1#47#85#diseaseC3489791 associated_with G2019S,autosomal dominant Parkinson's disease

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
16240353-0#7#12#gene120892 7-12 gene120892 denotes LRRK2
16240353-0#64#83#diseaseC0030567 64-83 diseaseC0030567 denotes Parkinson's disease
16240353-6#0#5#gene120892 664-669 gene120892 denotes LRRK2
16240353-6#66#68#diseaseC3489791 730-732 diseaseC3489791 denotes PD
7#12#gene12089264#83#diseaseC0030567 16240353-0#7#12#gene120892 16240353-0#64#83#diseaseC0030567 associated_with LRRK2,Parkinson's disease
0#5#gene12089266#68#diseaseC3489791 16240353-6#0#5#gene120892 16240353-6#66#68#diseaseC3489791 associated_with LRRK2,PD