PMC:1440874 / 126-472 JSONTXT

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    craft-sa-dev

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Mice Lacking Atrx\n\nAbstract\nATRX is an X-encoded member of the SNF2 family of ATPase/helicase proteins thought to regulate gene expression by modifying chromatin at target loci. Mutations in ATRX provided the first example of a human genetic disease associated with defects in such proteins. To better understand the role of ATRX in development "}

    craft-ca-core-ex-dev

    {"project":"craft-ca-core-ex-dev","denotations":[{"id":"T97","span":{"begin":29,"end":33},"obj":"PR_EXT:000004503"},{"id":"T98","span":{"begin":40,"end":41},"obj":"GO:0000805"},{"id":"T99","span":{"begin":42,"end":49},"obj":"SO_EXT:sequence_coding_function"},{"id":"T100","span":{"begin":64,"end":68},"obj":"PR_EXT:P22082"},{"id":"T101","span":{"begin":79,"end":85},"obj":"GO_EXT:0016887"},{"id":"T102","span":{"begin":86,"end":94},"obj":"GO_EXT:0004386"},{"id":"T103","span":{"begin":95,"end":103},"obj":"CHEBI_PR_EXT:protein"},{"id":"T104","span":{"begin":115,"end":123},"obj":"GO:0065007"},{"id":"T105","span":{"begin":124,"end":128},"obj":"SO_EXT:0000704"},{"id":"T106","span":{"begin":124,"end":139},"obj":"GO:0010467"},{"id":"T107","span":{"begin":153,"end":162},"obj":"GO:0000785"},{"id":"T108","span":{"begin":179,"end":188},"obj":"SO_EXT:sequence_alteration_entity_or_process"},{"id":"T109","span":{"begin":192,"end":196},"obj":"PR_EXT:000004503"},{"id":"T110","span":{"begin":229,"end":234},"obj":"NCBITaxon:9606"},{"id":"T111","span":{"begin":235,"end":242},"obj":"SO_EXT:0000704"},{"id":"T112","span":{"begin":283,"end":291},"obj":"CHEBI_PR_EXT:protein"},{"id":"T113","span":{"begin":326,"end":330},"obj":"PR_EXT:000004503"}],"text":" Mice Lacking Atrx\n\nAbstract\nATRX is an X-encoded member of the SNF2 family of ATPase/helicase proteins thought to regulate gene expression by modifying chromatin at target loci. Mutations in ATRX provided the first example of a human genetic disease associated with defects in such proteins. To better understand the role of ATRX in development "}

    craft-ca-core-dev

    {"project":"craft-ca-core-dev","denotations":[{"id":"T53","span":{"begin":29,"end":33},"obj":"PR:000004503"},{"id":"T54","span":{"begin":40,"end":41},"obj":"GO:0000805"},{"id":"T55","span":{"begin":64,"end":68},"obj":"PR:P22082"},{"id":"T56","span":{"begin":115,"end":123},"obj":"GO:0065007"},{"id":"T57","span":{"begin":124,"end":128},"obj":"SO:0000704"},{"id":"T58","span":{"begin":124,"end":139},"obj":"GO:0010467"},{"id":"T59","span":{"begin":153,"end":162},"obj":"GO:0000785"},{"id":"T60","span":{"begin":192,"end":196},"obj":"PR:000004503"},{"id":"T61","span":{"begin":229,"end":234},"obj":"NCBITaxon:9606"},{"id":"T62","span":{"begin":235,"end":242},"obj":"SO:0000704"},{"id":"T63","span":{"begin":326,"end":330},"obj":"PR:000004503"}],"text":" Mice Lacking Atrx\n\nAbstract\nATRX is an X-encoded member of the SNF2 family of ATPase/helicase proteins thought to regulate gene expression by modifying chromatin at target loci. Mutations in ATRX provided the first example of a human genetic disease associated with defects in such proteins. To better understand the role of ATRX in development "}