PMC:1892049 / 7151-7419 JSONTXT

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    craft-ca-core-ex-dev

    {"project":"craft-ca-core-ex-dev","denotations":[{"id":"T6113","span":{"begin":10,"end":25},"obj":"SO_EXT:0005858"},{"id":"T6114","span":{"begin":33,"end":38},"obj":"NCBITaxon:9606"},{"id":"T6115","span":{"begin":39,"end":45},"obj":"SO_EXT:0001026"},{"id":"T6116","span":{"begin":67,"end":75},"obj":"SO_EXT:sequence_alteration_entity_or_process"},{"id":"T6117","span":{"begin":107,"end":112},"obj":"UBERON:0007023"},{"id":"T6119","span":{"begin":195,"end":203},"obj":"SO_EXT:missense_quality_or_entity"},{"id":"T6120","span":{"begin":204,"end":212},"obj":"SO_EXT:sequence_alteration_entity_or_process"},{"id":"T6121","span":{"begin":216,"end":221},"obj":"PR_EXT:000009158"},{"id":"T6118","span":{"begin":119,"end":128},"obj":"GO:0030849"}],"text":"ed to the syntenic region of the human genome, but where no causal mutation had been identified. SCA15, an adult-onset autosomal dominant progressive ataxia is linked to this locus [5]. Although missense mutation of ITPR1 had previously been ruled out [2] and the mode"}

    craft-ca-core-dev

    {"project":"craft-ca-core-dev","denotations":[{"id":"T5871","span":{"begin":10,"end":25},"obj":"SO:0005858"},{"id":"T5872","span":{"begin":33,"end":38},"obj":"NCBITaxon:9606"},{"id":"T5873","span":{"begin":39,"end":45},"obj":"SO:0001026"},{"id":"T5874","span":{"begin":107,"end":112},"obj":"UBERON:0007023"},{"id":"T5875","span":{"begin":119,"end":128},"obj":"GO:0030849"},{"id":"T5876","span":{"begin":216,"end":221},"obj":"PR:000009158"}],"text":"ed to the syntenic region of the human genome, but where no causal mutation had been identified. SCA15, an adult-onset autosomal dominant progressive ataxia is linked to this locus [5]. Although missense mutation of ITPR1 had previously been ruled out [2] and the mode"}

    craft-sa-dev

    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to the syntenic region of the human genome, but where no causal mutation had been identified. SCA15, an adult-onset autosomal dominant progressive ataxia is linked to this locus [5]. Although missense mutation of ITPR1 had previously been ruled out [2] and the mode"}

    2_test

    {"project":"2_test","denotations":[{"id":"17590087-11723290-85657848","span":{"begin":182,"end":183},"obj":"11723290"},{"id":"17590087-12828938-85657849","span":{"begin":253,"end":254},"obj":"12828938"},{"id":"T90169","span":{"begin":182,"end":183},"obj":"11723290"},{"id":"T64459","span":{"begin":253,"end":254},"obj":"12828938"}],"text":"ed to the syntenic region of the human genome, but where no causal mutation had been identified. SCA15, an adult-onset autosomal dominant progressive ataxia is linked to this locus [5]. Although missense mutation of ITPR1 had previously been ruled out [2] and the mode"}