PubMed:19545277 / 167-304 JSONTXT

Annnotations TAB JSON ListView MergeView

    c_corpus

    {"project":"c_corpus","denotations":[{"id":"T17","span":{"begin":32,"end":39},"obj":"6308"},{"id":"T18","span":{"begin":32,"end":39},"obj":"SO:0001437"},{"id":"T16","span":{"begin":32,"end":39},"obj":"CHEBI:15603"},{"id":"T19","span":{"begin":32,"end":39},"obj":"D007930"},{"id":"T20","span":{"begin":32,"end":39},"obj":"CHEBI:25017"},{"id":"T21","span":{"begin":32,"end":39},"obj":"D007930"},{"id":"T22","span":{"begin":45,"end":51},"obj":"SO:0001068"},{"id":"T23","span":{"begin":62,"end":67},"obj":"PR:Q5S006"},{"id":"T24","span":{"begin":62,"end":67},"obj":"PR:000003033"},{"id":"T25","span":{"begin":62,"end":67},"obj":"PR:Q5S007"},{"id":"T26","span":{"begin":106,"end":116},"obj":"D000067562"},{"id":"T27","span":{"begin":106,"end":116},"obj":"D000067562"},{"id":"T32","span":{"begin":117,"end":136},"obj":"D010300"},{"id":"T33","span":{"begin":117,"end":136},"obj":"D010300"}],"text":"Autosomal dominant mutations in leucine-rich repeat kinase 2 (LRRK2) are the most common genetic cause of late-onset Parkinson's disease."}

    UseCases_ArguminSci_Discourse

    {"project":"UseCases_ArguminSci_Discourse","denotations":[{"id":"T2","span":{"begin":0,"end":137},"obj":"DRI_Background"}],"text":"Autosomal dominant mutations in leucine-rich repeat kinase 2 (LRRK2) are the most common genetic cause of late-onset Parkinson's disease."}

    PubMed_ArguminSci

    {"project":"PubMed_ArguminSci","denotations":[{"id":"T1","span":{"begin":0,"end":137},"obj":"DRI_Background"}],"text":"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

    {"project":"DisGeNET5_gene_disease","denotations":[{"id":"19545277-1#32#60#gene120892","span":{"begin":32,"end":60},"obj":"gene120892"},{"id":"19545277-1#62#67#gene120892","span":{"begin":62,"end":67},"obj":"gene120892"},{"id":"19545277-1#106#136#diseaseC3160718","span":{"begin":106,"end":136},"obj":"diseaseC3160718"}],"relations":[{"id":"32#60#gene120892106#136#diseaseC3160718","pred":"associated_with","subj":"19545277-1#32#60#gene120892","obj":"19545277-1#106#136#diseaseC3160718"},{"id":"62#67#gene120892106#136#diseaseC3160718","pred":"associated_with","subj":"19545277-1#62#67#gene120892","obj":"19545277-1#106#136#diseaseC3160718"}],"text":"Autosomal dominant mutations in leucine-rich repeat kinase 2 (LRRK2) are the most common genetic cause of late-onset Parkinson's disease."}