PMC:1186732 / 559-666 JSONTXT

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{"project":"craft-ca-core-ex-dev","denotations":[{"id":"T130","span":{"begin":1,"end":7},"obj":"SO_EXT:sequence_altered_entity"},{"id":"T131","span":{"begin":30,"end":38},"obj":"SO_EXT:sequence_deletion_entity_or_process"},{"id":"T132","span":{"begin":46,"end":51},"obj":"NCBITaxon:10088"},{"id":"T133","span":{"begin":52,"end":60},"obj":"SO_EXT:0000855"},{"id":"T134","span":{"begin":64,"end":69},"obj":"PR_EXT:000011403"},{"id":"T135","span":{"begin":74,"end":80},"obj":"SO:0000910"},{"id":"T136","span":{"begin":81,"end":88},"obj":"GO:0005634"},{"id":"T137","span":{"begin":89,"end":97},"obj":"GO_EXT:0004872"}],"text":" mutant carries a spontaneous deletion in the mouse ortholog of NR2E3, an orphan nuclear receptor transcrip"}

{"project":"craft-ca-core-dev","denotations":[{"id":"T73","span":{"begin":46,"end":51},"obj":"NCBITaxon:10088"},{"id":"T74","span":{"begin":52,"end":60},"obj":"SO:0000855"},{"id":"T75","span":{"begin":64,"end":69},"obj":"PR:000011403"},{"id":"T76","span":{"begin":74,"end":80},"obj":"SO:0000910"},{"id":"T77","span":{"begin":81,"end":88},"obj":"GO:0005634"}],"text":" mutant carries a spontaneous deletion in the mouse ortholog of NR2E3, an orphan nuclear receptor transcrip"}