PMC:1892049 / 814-985 JSONTXT

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    craft-ca-core-ex-dev

    {"project":"craft-ca-core-ex-dev","denotations":[{"id":"T853","span":{"begin":8,"end":13},"obj":"CL_GO_EXT:cell"},{"id":"T854","span":{"begin":15,"end":30},"obj":"UBERON:0014643"},{"id":"T855","span":{"begin":52,"end":57},"obj":"NCBITaxon:9606"},{"id":"T856","span":{"begin":58,"end":67},"obj":"GO:0030849"},{"id":"T857","span":{"begin":99,"end":106},"obj":"SO_EXT:0001026"},{"id":"T858","span":{"begin":125,"end":130},"obj":"PR_EXT:000009158"},{"id":"T859","span":{"begin":159,"end":168},"obj":"SO_EXT:sequence_alteration_entity_or_process"}],"text":"urkinje cells. Spinocerebellar ataxia 15 (SCA15), a human autosomal dominant disorder, maps to the genomic region containing ITPR1; however, to date no causal mutations ha"}

    craft-ca-core-dev

    {"project":"craft-ca-core-dev","denotations":[{"id":"T809","span":{"begin":15,"end":30},"obj":"UBERON:0014643"},{"id":"T810","span":{"begin":52,"end":57},"obj":"NCBITaxon:9606"},{"id":"T811","span":{"begin":58,"end":67},"obj":"GO:0030849"},{"id":"T812","span":{"begin":99,"end":106},"obj":"SO:0001026"},{"id":"T813","span":{"begin":125,"end":130},"obj":"PR:000009158"}],"text":"urkinje cells. Spinocerebellar ataxia 15 (SCA15), a human autosomal dominant disorder, maps to the genomic region containing ITPR1; however, to date no causal mutations ha"}

    craft-sa-dev

    {"project":"craft-sa-dev","denotations":[{"id":"T1020","span":{"begin":8,"end":13},"obj":"NNS"},{"id":"T1022","span":{"begin":13,"end":14},"obj":"."},{"id":"T1024","span":{"begin":15,"end":30},"obj":"JJ"},{"id":"T1025","span":{"begin":31,"end":37},"obj":"NN"},{"id":"T1026","span":{"begin":87,"end":91},"obj":"VBZ"},{"id":"T1027","span":{"begin":38,"end":40},"obj":"CD"},{"id":"T1028","span":{"begin":41,"end":42},"obj":"-LRB-"},{"id":"T1029","span":{"begin":42,"end":47},"obj":"NN"},{"id":"T1030","span":{"begin":47,"end":48},"obj":"-RRB-"},{"id":"T1031","span":{"begin":48,"end":50},"obj":","},{"id":"T1032","span":{"begin":50,"end":51},"obj":"DT"},{"id":"T1033","span":{"begin":77,"end":85},"obj":"NN"},{"id":"T1034","span":{"begin":52,"end":57},"obj":"JJ"},{"id":"T1035","span":{"begin":58,"end":67},"obj":"JJ"},{"id":"T1036","span":{"begin":68,"end":76},"obj":"JJ"},{"id":"T1037","span":{"begin":85,"end":87},"obj":","},{"id":"T1039","span":{"begin":92,"end":94},"obj":"IN"},{"id":"T1040","span":{"begin":95,"end":98},"obj":"DT"},{"id":"T1041","span":{"begin":107,"end":113},"obj":"NN"},{"id":"T1042","span":{"begin":99,"end":106},"obj":"JJ"},{"id":"T1043","span":{"begin":114,"end":124},"obj":"VBG"},{"id":"T1044","span":{"begin":125,"end":130},"obj":"NN"},{"id":"T1045","span":{"begin":130,"end":131},"obj":":"},{"id":"T1046","span":{"begin":132,"end":139},"obj":"RB"},{"id":"T1047","span":{"begin":139,"end":141},"obj":","},{"id":"T1048","span":{"begin":141,"end":143},"obj":"IN"},{"id":"T1049","span":{"begin":144,"end":148},"obj":"NN"},{"id":"T1050","span":{"begin":149,"end":151},"obj":"DT"},{"id":"T1051","span":{"begin":159,"end":168},"obj":"NNS"},{"id":"T1052","span":{"begin":152,"end":158},"obj":"JJ"}],"relations":[{"id":"R141","pred":"amod","subj":"T1024","obj":"T1025"},{"id":"R142","pred":"nsubj","subj":"T1025","obj":"T1026"},{"id":"R144","pred":"nummod","subj":"T1027","obj":"T1025"},{"id":"R145","pred":"punct","subj":"T1028","obj":"T1025"},{"id":"R146","pred":"appos","subj":"T1029","obj":"T1025"},{"id":"R147","pred":"punct","subj":"T1030","obj":"T1025"},{"id":"R148","pred":"punct","subj":"T1031","obj":"T1025"},{"id":"R149","pred":"det","subj":"T1032","obj":"T1033"},{"id":"R151","pred":"amod","subj":"T1034","obj":"T1033"},{"id":"R152","pred":"amod","subj":"T1035","obj":"T1033"},{"id":"R153","pred":"amod","subj":"T1036","obj":"T1033"},{"id":"R154","pred":"punct","subj":"T1037","obj":"T1026"},{"id":"R155","pred":"prep","subj":"T1039","obj":"T1026"},{"id":"R156","pred":"det","subj":"T1040","obj":"T1041"},{"id":"R157","pred":"pobj","subj":"T1041","obj":"T1039"},{"id":"R158","pred":"amod","subj":"T1042","obj":"T1041"},{"id":"R159","pred":"acl","subj":"T1043","obj":"T1041"},{"id":"R160","pred":"dobj","subj":"T1044","obj":"T1043"},{"id":"R165","pred":"pobj","subj":"T1049","obj":"T1048"},{"id":"R166","pred":"det","subj":"T1050","obj":"T1051"},{"id":"R168","pred":"amod","subj":"T1052","obj":"T1051"},{"id":"R150","pred":"appos","subj":"T1033","obj":"T1025"}],"text":"urkinje cells. Spinocerebellar ataxia 15 (SCA15), a human autosomal dominant disorder, maps to the genomic region containing ITPR1; however, to date no causal mutations ha"}

    Biotea

    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cells. Spinocerebellar ataxia 15 (SCA15), a human autosomal dominant disorder, maps to the genomic region containing ITPR1; however, to date no causal mutations ha"}