PMC:1166548 / 4499-4640 JSONTXT

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{"project":"craft-ca-core-ex-dev","denotations":[{"id":"T756","span":{"begin":1,"end":7},"obj":"CHEBI_SO_EXT:molecular_indicator_or_label_or_marker_or_tag"},{"id":"T757","span":{"begin":8,"end":18},"obj":"SO_EXT:0001024"},{"id":"T758","span":{"begin":26,"end":41},"obj":"SO_EXT:0005858"},{"id":"T759","span":{"begin":35,"end":44},"obj":"_FRAGMENT"},{"id":"T760","span":{"begin":51,"end":61},"obj":"GO_SO_EXT:chromosomal_part_or_position_or_region_or_site"},{"id":"T761","span":{"begin":45,"end":50},"obj":"NCBITaxon:9606"}],"relations":[{"id":"R377","pred":"_lexicallyChainedTo","subj":"T760","obj":"T759"}],"text":" Marker haplotypes of the syntenic region of human chromosome 19q13 were also shown to be associated with the risk of MI in CF patients [18]."}

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