PMC:1186732 / 419-652 JSONTXT

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    craft-sa-dev

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    craft-ca-core-ex-dev

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    craft-ca-core-dev

    {"project":"craft-ca-core-dev","denotations":[{"id":"T68","span":{"begin":11,"end":30},"obj":"CL:0000210"},{"id":"T69","span":{"begin":38,"end":45},"obj":"UBERON:0000966"},{"id":"T70","span":{"begin":74,"end":79},"obj":"NCBITaxon:10088"},{"id":"T71","span":{"begin":97,"end":102},"obj":"NCBITaxon:9606"},{"id":"T72","span":{"begin":114,"end":118},"obj":"CL:0000573"},{"id":"T73","span":{"begin":186,"end":191},"obj":"NCBITaxon:10088"},{"id":"T74","span":{"begin":192,"end":200},"obj":"SO:0000855"},{"id":"T75","span":{"begin":204,"end":209},"obj":"PR:000011403"},{"id":"T76","span":{"begin":214,"end":220},"obj":"SO:0000910"},{"id":"T77","span":{"begin":221,"end":228},"obj":"GO:0005634"}],"text":"amined the photoreceptor cells of the retinal degeneration 7 (rd7) mutant mouse, a model for the human enhanced S-cone syndrome (ESCS). This mutant carries a spontaneous deletion in the mouse ortholog of NR2E3, an orphan nuclear rece"}