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{"project":"craft-ca-core-dev","denotations":[{"id":"T22","span":{"begin":103,"end":110},"obj":"SO:0001023"},{"id":"T23","span":{"begin":123,"end":127},"obj":"SO:0000704"},{"id":"T24","span":{"begin":142,"end":147},"obj":"NCBITaxon:9606"}],"text":"ty at theXpd Locus\n\nAbstract\nAlthough compound heterozygosity, or the presence of two different mutant alleles of the same gene, is common in human recessive disease, its potential to impact disease outcome has not been well do"}

{"project":"craft-ca-core-ex-dev","denotations":[{"id":"T51","span":{"begin":96,"end":102},"obj":"SO_EXT:sequence_altered_entity_or_alteration_process"},{"id":"T52","span":{"begin":103,"end":110},"obj":"SO_EXT:0001023"},{"id":"T53","span":{"begin":123,"end":127},"obj":"SO_EXT:0000704"},{"id":"T54","span":{"begin":142,"end":147},"obj":"NCBITaxon:9606"}],"text":"ty at theXpd Locus\n\nAbstract\nAlthough compound heterozygosity, or the presence of two different mutant alleles of the same gene, is common in human recessive disease, its potential to impact disease outcome has not been well do"}