PubMed:26994442 / 0-240 JSONTXT

{"project":"c_corpus","denotations":[{"id":"T2","span":{"begin":22,"end":25},"obj":"CHEBI:16768"},{"id":"T6","span":{"begin":22,"end":25},"obj":"D009074"},{"id":"T7","span":{"begin":22,"end":25},"obj":"D009074"},{"id":"T8","span":{"begin":22,"end":26},"obj":"PR:O65607"},{"id":"T9","span":{"begin":22,"end":26},"obj":"PR:000010667"},{"id":"T10","span":{"begin":22,"end":26},"obj":"PR:Q59Y41"},{"id":"T11","span":{"begin":22,"end":26},"obj":"PR:P25336"},{"id":"T12","span":{"begin":22,"end":26},"obj":"PR:P20585"},{"id":"T13","span":{"begin":22,"end":26},"obj":"PR:P26359"},{"id":"T14","span":{"begin":22,"end":26},"obj":"PR:P13705"},{"id":"T15","span":{"begin":22,"end":26},"obj":"PR:Q1ZXH0"},{"id":"T16","span":{"begin":27,"end":42},"obj":"GO:0006298"},{"id":"T17","span":{"begin":43,"end":47},"obj":"SO:0000704"},{"id":"T18","span":{"begin":121,"end":127},"obj":"SO:0001068"},{"id":"T21","span":{"begin":141,"end":144},"obj":"SO:0000352"},{"id":"T20","span":{"begin":141,"end":144},"obj":"CHEBI:16991"},{"id":"T22","span":{"begin":141,"end":144},"obj":"D004247"},{"id":"T19","span":{"begin":141,"end":144},"obj":"GO:0005574"},{"id":"T23","span":{"begin":148,"end":166},"obj":"D009223"},{"id":"T24","span":{"begin":148,"end":166},"obj":"D009223"},{"id":"T25","span":{"begin":222,"end":228},"obj":"SO:0001068"}],"text":"A polymorphism in the MSH3 mismatch repair gene is associated with the levels of somatic instability of the expanded CTG repeat in the blood DNA of myotonic dystrophy type 1 patients.\nSomatic mosaicism of the expanded CTG repeat in myotonic"}

{"project":"DisGeNET5_gene_disease","denotations":[{"id":"26994442-0#22#26#gene4437","span":{"begin":22,"end":26},"obj":"gene4437"},{"id":"26994442-0#148#166#diseaseC0027126","span":{"begin":148,"end":166},"obj":"diseaseC0027126"}],"relations":[{"id":"22#26#gene4437148#166#diseaseC0027126","pred":"associated_with","subj":"26994442-0#22#26#gene4437","obj":"26994442-0#148#166#diseaseC0027126"}],"text":"A polymorphism in the MSH3 mismatch repair gene is associated with the levels of somatic instability of the expanded CTG repeat in the blood DNA of myotonic dystrophy type 1 patients.\nSomatic mosaicism of the expanded CTG repeat in myotonic"}