PMC:1584416 / 211-276 JSONTXT

{"project":"craft-sa-dev","denotations":[{"id":"T97","span":{"begin":14,"end":16},"obj":"VBZ"},{"id":"T111","span":{"begin":8,"end":12},"obj":"NN"},{"id":"T112","span":{"begin":3,"end":7},"obj":"JJ"},{"id":"T113","span":{"begin":12,"end":14},"obj":","},{"id":"T115","span":{"begin":17,"end":23},"obj":"JJ"},{"id":"T116","span":{"begin":24,"end":26},"obj":"IN"},{"id":"T117","span":{"begin":27,"end":32},"obj":"JJ"},{"id":"T118","span":{"begin":43,"end":50},"obj":"NN"},{"id":"T119","span":{"begin":33,"end":42},"obj":"JJ"},{"id":"T120","span":{"begin":50,"end":52},"obj":","},{"id":"T121","span":{"begin":52,"end":55},"obj":"PRP$"},{"id":"T122","span":{"begin":56,"end":65},"obj":"NN"}],"relations":[{"id":"R26","pred":"amod","subj":"T112","obj":"T111"},{"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":"R34","pred":"poss","subj":"T121","obj":"T122"},{"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":"he same gene, is common in human recessive disease, its potential"}

{"project":"craft-ca-core-dev","denotations":[{"id":"T23","span":{"begin":8,"end":12},"obj":"SO:0000704"},{"id":"T24","span":{"begin":27,"end":32},"obj":"NCBITaxon:9606"}],"text":"he same gene, is common in human recessive disease, its potential"}

{"project":"craft-ca-core-ex-dev","denotations":[{"id":"T53","span":{"begin":8,"end":12},"obj":"SO_EXT:0000704"},{"id":"T54","span":{"begin":27,"end":32},"obj":"NCBITaxon:9606"}],"text":"he same gene, is common in human recessive disease, its potential"}