PMC:539297 / 207-443 JSONTXT

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    craft-ca-core-dev

    {"project":"craft-ca-core-dev","denotations":[{"id":"T65","span":{"begin":73,"end":77},"obj":"PR:000005591"},{"id":"T66","span":{"begin":110,"end":118},"obj":"PR:000005591"},{"id":"T67","span":{"begin":151,"end":164},"obj":"GO:0005739"},{"id":"T68","span":{"begin":151,"end":188},"obj":"PR:000022190"},{"id":"T69","span":{"begin":212,"end":215},"obj":"UBERON:0001017"},{"id":"T70","span":{"begin":212,"end":223},"obj":"CL:0000117"}],"text":"hildhood-onset neurodegenerative disease most-commonly caused by a ~1 kb CLN3 mutation. The resulting loss of battenin activity leads to deposition of mitochondrial ATP synthase, subunit c and a specific loss of CNS neurons. We previous"}

    craft-sa-dev

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    craft-ca-core-ex-dev

    {"project":"craft-ca-core-ex-dev","denotations":[{"id":"T111","span":{"begin":71,"end":72},"obj":"CHEBI_SO_EXT:base"},{"id":"T112","span":{"begin":73,"end":77},"obj":"PR_EXT:000005591"},{"id":"T113","span":{"begin":78,"end":86},"obj":"SO_EXT:sequence_alteration_entity_or_process"},{"id":"T114","span":{"begin":110,"end":118},"obj":"PR_EXT:000005591"},{"id":"T115","span":{"begin":151,"end":164},"obj":"GO:0005739"},{"id":"T116","span":{"begin":151,"end":188},"obj":"PR_EXT:000022190"},{"id":"T117","span":{"begin":165,"end":168},"obj":"CHEBI_EXT:ATP"},{"id":"T118","span":{"begin":212,"end":215},"obj":"UBERON:0001017"},{"id":"T119","span":{"begin":212,"end":223},"obj":"CL:0000117"}],"text":"hildhood-onset neurodegenerative disease most-commonly caused by a ~1 kb CLN3 mutation. The resulting loss of battenin activity leads to deposition of mitochondrial ATP synthase, subunit c and a specific loss of CNS neurons. We previous"}