PubMed:17409200 / 0-258 JSONTXT

{"project":"c_corpus","denotations":[{"id":"T1","span":{"begin":8,"end":14},"obj":"SO:0001068"},{"id":"T2","span":{"begin":15,"end":23},"obj":"SO:0000109"},{"id":"T5","span":{"begin":88,"end":106},"obj":"D006816"},{"id":"T6","span":{"begin":88,"end":106},"obj":"D006816"},{"id":"T9","span":{"begin":107,"end":112},"obj":"UBERON:6110636"},{"id":"T10","span":{"begin":107,"end":112},"obj":"UBERON:0000955"},{"id":"T11","span":{"begin":125,"end":132},"obj":"D004194"},{"id":"T12","span":{"begin":125,"end":132},"obj":"D004194"},{"id":"T13","span":{"begin":165,"end":168},"obj":"CVCL_D569"},{"id":"T14","span":{"begin":169,"end":175},"obj":"SO:0001068"},{"id":"T19","span":{"begin":197,"end":206},"obj":"4885"},{"id":"T15","span":{"begin":197,"end":206},"obj":"SO:0001448"},{"id":"T16","span":{"begin":197,"end":206},"obj":"D005973"},{"id":"T17","span":{"begin":197,"end":206},"obj":"CHEBI:28300"},{"id":"T18","span":{"begin":197,"end":206},"obj":"CHEBI:18050"},{"id":"T20","span":{"begin":197,"end":206},"obj":"D005973"},{"id":"T21","span":{"begin":207,"end":212},"obj":"UBERON:0001018"},{"id":"T26","span":{"begin":218,"end":225},"obj":"SO:0000104"},{"id":"T25","span":{"begin":218,"end":225},"obj":"PR:000000001"},{"id":"T22","span":{"begin":218,"end":225},"obj":"GO:0003675"},{"id":"T23","span":{"begin":218,"end":225},"obj":"CHEBI:36080"},{"id":"T24","span":{"begin":218,"end":225},"obj":"CHEBI:11122"},{"id":"T27","span":{"begin":233,"end":243},"obj":"P42858"},{"id":"T28","span":{"begin":233,"end":243},"obj":"P42859"},{"id":"T29","span":{"begin":233,"end":243},"obj":"P51111"},{"id":"T30","span":{"begin":233,"end":243},"obj":"PR:000008840"},{"id":"T31","span":{"begin":233,"end":243},"obj":"P51112"}],"text":"Triplet repeat mutation length gains correlate with cell-type specific vulnerability in Huntington disease brain.\nHuntington disease is caused by the expansion of a CAG repeat encoding an extended glutamine tract in a protein called huntingtin. Here, we prov"}

{"project":"UseCases_ArguminSci_Discourse","denotations":[{"id":"T1","span":{"begin":0,"end":113},"obj":"DRI_Outcome"},{"id":"T2","span":{"begin":114,"end":244},"obj":"DRI_Background"}],"text":"Triplet repeat mutation length gains correlate with cell-type specific vulnerability in Huntington disease brain.\nHuntington disease is caused by the expansion of a CAG repeat encoding an extended glutamine tract in a protein called huntingtin. Here, we prov"}