PMC:1208879 / 1681-1819 JSONTXT

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{"project":"craft-ca-core-ex-dev","denotations":[{"id":"T676","span":{"begin":14,"end":23},"obj":"SO_EXT:sequence_alteration_entity_or_process"},{"id":"T677","span":{"begin":31,"end":36},"obj":"NCBITaxon:9606"},{"id":"T678","span":{"begin":37,"end":41},"obj":"PR_EXT:000012318"},{"id":"T679","span":{"begin":42,"end":46},"obj":"SO_EXT:0000704"},{"id":"T680","span":{"begin":78,"end":82},"obj":"UBERON:0001769"},{"id":"T681","span":{"begin":116,"end":119},"obj":"UBERON:0000970"}],"text":" Heterozygous mutations of the human PAX6 gene cause aniridia (absence of the iris) and a range of other congenital eye malformations [2]."}

{"project":"craft-ca-core-dev","denotations":[{"id":"T557","span":{"begin":31,"end":36},"obj":"NCBITaxon:9606"},{"id":"T558","span":{"begin":37,"end":41},"obj":"PR:000012318"},{"id":"T559","span":{"begin":42,"end":46},"obj":"SO:0000704"},{"id":"T560","span":{"begin":78,"end":82},"obj":"UBERON:0001769"},{"id":"T561","span":{"begin":116,"end":119},"obj":"UBERON:0000970"}],"text":" Heterozygous mutations of the human PAX6 gene cause aniridia (absence of the iris) and a range of other congenital eye malformations [2]."}