PMC:1584416 / 2195-2523 JSONTXT

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    craft-sa-dev

    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Evidence of interallelic complementation at clinically relevant loci is limited to biochemical and cell-based studies of a handful of metabolic disorders with defects in enzymes including propinyl-CoA carboxylase [2], argininosuccinate lyase [3], galactose-1-phosphate uridylyltransferase [4], and methylmalonyl CoA mutase [5]."}

    craft-ca-core-dev

    {"project":"craft-ca-core-dev","denotations":[{"id":"T410","span":{"begin":18,"end":25},"obj":"SO:0001023"},{"id":"T411","span":{"begin":135,"end":144},"obj":"GO:0008152"},{"id":"T412","span":{"begin":189,"end":201},"obj":"CHEBI:15539"},{"id":"T413","span":{"begin":219,"end":236},"obj":"CHEBI:57472"},{"id":"T414","span":{"begin":248,"end":269},"obj":"CHEBI:53025"},{"id":"T415","span":{"begin":299,"end":316},"obj":"CHEBI:16625"}],"text":" Evidence of interallelic complementation at clinically relevant loci is limited to biochemical and cell-based studies of a handful of metabolic disorders with defects in enzymes including propinyl-CoA carboxylase [2], argininosuccinate lyase [3], galactose-1-phosphate uridylyltransferase [4], and methylmalonyl CoA mutase [5]."}

    craft-ca-core-ex-dev

    {"project":"craft-ca-core-ex-dev","denotations":[{"id":"T470","span":{"begin":18,"end":25},"obj":"SO_EXT:0001023"},{"id":"T471","span":{"begin":84,"end":95},"obj":"CHEBI_EXT:biochemical"},{"id":"T472","span":{"begin":100,"end":104},"obj":"CL_GO_EXT:cell"},{"id":"T473","span":{"begin":135,"end":144},"obj":"GO:0008152"},{"id":"T474","span":{"begin":171,"end":178},"obj":"CHEBI_GO_SO_EXT:enzyme"},{"id":"T475","span":{"begin":189,"end":201},"obj":"CHEBI:15539"},{"id":"T476","span":{"begin":189,"end":213},"obj":"GO_EXT:0004658"},{"id":"T477","span":{"begin":219,"end":236},"obj":"CHEBI:57472"},{"id":"T478","span":{"begin":219,"end":242},"obj":"GO_PR_EXT:argininosuccinate_lyase"},{"id":"T479","span":{"begin":248,"end":269},"obj":"CHEBI:53025"},{"id":"T480","span":{"begin":248,"end":289},"obj":"GO_PR_EXT:galactose_1_phosphate_uridylyltransferase"},{"id":"T481","span":{"begin":299,"end":316},"obj":"CHEBI:16625"},{"id":"T482","span":{"begin":299,"end":323},"obj":"GO_PR_EXT:methylmalonyl_CoA_mutase"}],"text":" Evidence of interallelic complementation at clinically relevant loci is limited to biochemical and cell-based studies of a handful of metabolic disorders with defects in enzymes including propinyl-CoA carboxylase [2], argininosuccinate lyase [3], galactose-1-phosphate uridylyltransferase [4], and methylmalonyl CoA mutase [5]."}

    2_test

    {"project":"2_test","denotations":[{"id":"17020410-8023851-84795120","span":{"begin":215,"end":216},"obj":"8023851"},{"id":"17020410-6589607-84795121","span":{"begin":244,"end":245},"obj":"6589607"},{"id":"17020410-8692963-84795122","span":{"begin":291,"end":292},"obj":"8692963"},{"id":"17020410-7909321-84795123","span":{"begin":325,"end":326},"obj":"7909321"},{"id":"T80536","span":{"begin":215,"end":216},"obj":"8023851"},{"id":"T45327","span":{"begin":244,"end":245},"obj":"6589607"},{"id":"T57048","span":{"begin":291,"end":292},"obj":"8692963"},{"id":"T8272","span":{"begin":325,"end":326},"obj":"7909321"}],"text":" Evidence of interallelic complementation at clinically relevant loci is limited to biochemical and cell-based studies of a handful of metabolic disorders with defects in enzymes including propinyl-CoA carboxylase [2], argininosuccinate lyase [3], galactose-1-phosphate uridylyltransferase [4], and methylmalonyl CoA mutase [5]."}