PMC:1626108 / 1232-1516
Annnotations
craft-sa-dev
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activity of Cox11 over HKI. To probe the physiological role of RanBP2 and its role in HKI function, a mouse model harboring a genetically disrupted RanBP2 locus was generated. RanBP2−/− are embryonically lethal, and haploinsufficiency of RanBP2 in an inbred strain causes a pronounce"}
craft-ca-core-ex-dev
{"project":"craft-ca-core-ex-dev","denotations":[{"id":"T190","span":{"begin":13,"end":18},"obj":"PR_EXT:000005770"},{"id":"T191","span":{"begin":24,"end":27},"obj":"PR_EXT:000008608"},{"id":"T192","span":{"begin":42,"end":55},"obj":"GO_PATO_EXT:physiological_process_or_quality"},{"id":"T193","span":{"begin":64,"end":70},"obj":"PR_EXT:000013712"},{"id":"T194","span":{"begin":87,"end":90},"obj":"PR_EXT:000008608"},{"id":"T195","span":{"begin":103,"end":108},"obj":"NCBITaxon:10088"},{"id":"T196","span":{"begin":127,"end":138},"obj":"SO_EXT:0000704"},{"id":"T197","span":{"begin":149,"end":155},"obj":"PR_EXT:000013712"},{"id":"T198","span":{"begin":177,"end":183},"obj":"PR_EXT:000013712"},{"id":"T199","span":{"begin":183,"end":184},"obj":"SO_EXT:sequence_nullness_or_absence"},{"id":"T200","span":{"begin":185,"end":186},"obj":"SO_EXT:sequence_nullness_or_absence"},{"id":"T201","span":{"begin":191,"end":204},"obj":"UBERON:0000922"},{"id":"T202","span":{"begin":205,"end":211},"obj":"GO_EXT:fatality_or_lethality"},{"id":"T203","span":{"begin":239,"end":245},"obj":"PR_EXT:000013712"}],"text":" activity of Cox11 over HKI. To probe the physiological role of RanBP2 and its role in HKI function, a mouse model harboring a genetically disrupted RanBP2 locus was generated. RanBP2−/− are embryonically lethal, and haploinsufficiency of RanBP2 in an inbred strain causes a pronounce"}
craft-ca-core-dev
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