PMC:1892049 / 814-985
Annnotations
craft-ca-core-ex-dev
{"project":"craft-ca-core-ex-dev","denotations":[{"id":"T853","span":{"begin":8,"end":13},"obj":"CL_GO_EXT:cell"},{"id":"T854","span":{"begin":15,"end":30},"obj":"UBERON:0014643"},{"id":"T855","span":{"begin":52,"end":57},"obj":"NCBITaxon:9606"},{"id":"T856","span":{"begin":58,"end":67},"obj":"GO:0030849"},{"id":"T857","span":{"begin":99,"end":106},"obj":"SO_EXT:0001026"},{"id":"T858","span":{"begin":125,"end":130},"obj":"PR_EXT:000009158"},{"id":"T859","span":{"begin":159,"end":168},"obj":"SO_EXT:sequence_alteration_entity_or_process"}],"text":"urkinje cells. Spinocerebellar ataxia 15 (SCA15), a human autosomal dominant disorder, maps to the genomic region containing ITPR1; however, to date no causal mutations ha"}
craft-ca-core-dev
{"project":"craft-ca-core-dev","denotations":[{"id":"T809","span":{"begin":15,"end":30},"obj":"UBERON:0014643"},{"id":"T810","span":{"begin":52,"end":57},"obj":"NCBITaxon:9606"},{"id":"T811","span":{"begin":58,"end":67},"obj":"GO:0030849"},{"id":"T812","span":{"begin":99,"end":106},"obj":"SO:0001026"},{"id":"T813","span":{"begin":125,"end":130},"obj":"PR:000009158"}],"text":"urkinje cells. Spinocerebellar ataxia 15 (SCA15), a human autosomal dominant disorder, maps to the genomic region containing ITPR1; however, to date no causal mutations ha"}
craft-sa-dev
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Biotea
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cells. 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