PMC:1584416 / 221-262 JSONTXT

{"project":"craft-sa-dev","denotations":[{"id":"T97","span":{"begin":4,"end":6},"obj":"VBZ"},{"id":"T113","span":{"begin":2,"end":4},"obj":","},{"id":"T115","span":{"begin":7,"end":13},"obj":"JJ"},{"id":"T116","span":{"begin":14,"end":16},"obj":"IN"},{"id":"T117","span":{"begin":17,"end":22},"obj":"JJ"},{"id":"T118","span":{"begin":33,"end":40},"obj":"NN"},{"id":"T119","span":{"begin":23,"end":32},"obj":"JJ"}],"relations":[{"id":"R27","pred":"punct","subj":"T113","obj":"T97"},{"id":"R31","pred":"pobj","subj":"T118","obj":"T116"},{"id":"R32","pred":"amod","subj":"T119","obj":"T118"},{"id":"R28","pred":"acomp","subj":"T115","obj":"T97"},{"id":"R29","pred":"prep","subj":"T116","obj":"T97"},{"id":"R30","pred":"amod","subj":"T117","obj":"T118"}],"text":"ne, is common in human recessive disease,"}

{"project":"craft-ca-core-dev","denotations":[{"id":"T24","span":{"begin":17,"end":22},"obj":"NCBITaxon:9606"}],"text":"ne, is common in human recessive disease,"}

{"project":"craft-ca-core-ex-dev","denotations":[{"id":"T54","span":{"begin":17,"end":22},"obj":"NCBITaxon:9606"}],"text":"ne, is common in human recessive disease,"}