PMC:1584416 / 31017-31159 JSONTXT

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{"project":"craft-ca-core-dev","denotations":[{"id":"T5542","span":{"begin":77,"end":83},"obj":"SO:0001023"},{"id":"T5543","span":{"begin":120,"end":123},"obj":"PR:000007164"}],"text":" Furthermore, XPTTD patient XP38BR carried a “causative” TTD mutation in one allele and a novel point mutation encoding XPDL485P in the other."}

{"project":"craft-ca-core-ex-dev","denotations":[{"id":"T5592","span":{"begin":61,"end":69},"obj":"SO_EXT:sequence_alteration_entity_or_process"},{"id":"T5593","span":{"begin":77,"end":83},"obj":"SO_EXT:0001023"},{"id":"T5594","span":{"begin":96,"end":110},"obj":"SO_EXT:point_mutation_entity_or_process"},{"id":"T5595","span":{"begin":111,"end":119},"obj":"SO_EXT:sequence_coding_function"},{"id":"T5596","span":{"begin":120,"end":123},"obj":"PR_EXT:000007164"}],"text":" Furthermore, XPTTD patient XP38BR carried a “causative” TTD mutation in one allele and a novel point mutation encoding XPDL485P in the other."}