PubMed:26744328 / 0-182 JSONTXT

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    c_corpus

    {"project":"c_corpus","denotations":[{"id":"T1","span":{"begin":0,"end":11},"obj":"Q9Y6H5"},{"id":"T2","span":{"begin":0,"end":11},"obj":"PR:000015323"},{"id":"T3","span":{"begin":0,"end":11},"obj":"Q99ME3"},{"id":"T4","span":{"begin":30,"end":35},"obj":"PR:Q5S006"},{"id":"T5","span":{"begin":30,"end":35},"obj":"PR:000003033"},{"id":"T6","span":{"begin":30,"end":35},"obj":"PR:Q5S007"},{"id":"T11","span":{"begin":65,"end":84},"obj":"D010300"},{"id":"T12","span":{"begin":65,"end":84},"obj":"D010300"},{"id":"T16","span":{"begin":106,"end":113},"obj":"6308"},{"id":"T17","span":{"begin":106,"end":113},"obj":"SO:0001437"},{"id":"T15","span":{"begin":106,"end":113},"obj":"CHEBI:15603"},{"id":"T18","span":{"begin":106,"end":113},"obj":"D007930"},{"id":"T19","span":{"begin":106,"end":113},"obj":"CHEBI:25017"},{"id":"T20","span":{"begin":106,"end":113},"obj":"D007930"},{"id":"T21","span":{"begin":119,"end":125},"obj":"SO:0001068"},{"id":"T22","span":{"begin":136,"end":141},"obj":"PR:Q5S006"},{"id":"T23","span":{"begin":136,"end":141},"obj":"PR:000003033"},{"id":"T24","span":{"begin":136,"end":141},"obj":"PR:Q5S007"},{"id":"T26","span":{"begin":149,"end":180},"obj":"D020734"},{"id":"T27","span":{"begin":149,"end":180},"obj":"D020734"}],"text":"Synphilin-1 attenuates mutant LRRK2-induced neurodegeneration in Parkinson's disease models.\nMutations in leucine-rich repeat kinase 2 (LRRK2) cause autosomal-dominant Parkinsonism w"}

    DisGeNET5_gene_disease

    {"project":"DisGeNET5_gene_disease","denotations":[{"id":"26744328-0#0#11#gene9627","span":{"begin":0,"end":11},"obj":"gene9627"},{"id":"26744328-0#30#35#gene120892","span":{"begin":30,"end":35},"obj":"gene120892"},{"id":"26744328-0#65#84#diseaseC0030567","span":{"begin":65,"end":84},"obj":"diseaseC0030567"},{"id":"26744328-1#13#41#gene120892","span":{"begin":106,"end":134},"obj":"gene120892"},{"id":"26744328-1#43#48#gene120892","span":{"begin":136,"end":141},"obj":"gene120892"},{"id":"26744328-1#56#87#diseaseC0752098","span":{"begin":149,"end":180},"obj":"diseaseC0752098"}],"relations":[{"id":"0#11#gene962765#84#diseaseC0030567","pred":"associated_with","subj":"26744328-0#0#11#gene9627","obj":"26744328-0#65#84#diseaseC0030567"},{"id":"30#35#gene12089265#84#diseaseC0030567","pred":"associated_with","subj":"26744328-0#30#35#gene120892","obj":"26744328-0#65#84#diseaseC0030567"},{"id":"13#41#gene12089256#87#diseaseC0752098","pred":"associated_with","subj":"26744328-1#13#41#gene120892","obj":"26744328-1#56#87#diseaseC0752098"},{"id":"43#48#gene12089256#87#diseaseC0752098","pred":"associated_with","subj":"26744328-1#43#48#gene120892","obj":"26744328-1#56#87#diseaseC0752098"}],"text":"Synphilin-1 attenuates mutant LRRK2-induced neurodegeneration in Parkinson's disease models.\nMutations in leucine-rich repeat kinase 2 (LRRK2) cause autosomal-dominant Parkinsonism w"}