PMC:1166548 / 148-312
Annnotations
craft-sa-dev
{"project":"craft-sa-dev","denotations":[{"id":"T164","span":{"begin":20,"end":26},"obj":"VBN"},{"id":"T165","span":{"begin":1,"end":7},"obj":"JJ"},{"id":"T166","span":{"begin":8,"end":16},"obj":"NN"},{"id":"T167","span":{"begin":17,"end":19},"obj":"VBZ"},{"id":"T168","span":{"begin":136,"end":138},"obj":"VBZ"},{"id":"T169","span":{"begin":27,"end":29},"obj":"IN"},{"id":"T170","span":{"begin":30,"end":39},"obj":"NNS"},{"id":"T171","span":{"begin":40,"end":42},"obj":"IN"},{"id":"T172","span":{"begin":43,"end":46},"obj":"DT"},{"id":"T173","span":{"begin":106,"end":110},"obj":"NN"},{"id":"T174","span":{"begin":47,"end":53},"obj":"JJ"},{"id":"T175","span":{"begin":89,"end":98},"obj":"NN"},{"id":"T176","span":{"begin":54,"end":62},"obj":"NN"},{"id":"T177","span":{"begin":63,"end":76},"obj":"JJ"},{"id":"T178","span":{"begin":77,"end":88},"obj":"NN"},{"id":"T179","span":{"begin":99,"end":100},"obj":"-LRB-"},{"id":"T180","span":{"begin":100,"end":104},"obj":"NN"},{"id":"T181","span":{"begin":104,"end":105},"obj":"-RRB-"},{"id":"T182","span":{"begin":110,"end":112},"obj":","},{"id":"T183","span":{"begin":112,"end":115},"obj":"DT"},{"id":"T184","span":{"begin":116,"end":124},"obj":"NN"},{"id":"T185","span":{"begin":125,"end":127},"obj":"IN"},{"id":"T186","span":{"begin":128,"end":135},"obj":"NN"},{"id":"T187","span":{"begin":139,"end":145},"obj":"RB"},{"id":"T188","span":{"begin":146,"end":154},"obj":"JJ"}],"relations":[{"id":"R19","pred":"advcl","subj":"T164","obj":"T168"},{"id":"R23","pred":"agent","subj":"T169","obj":"T164"},{"id":"R24","pred":"pobj","subj":"T170","obj":"T169"},{"id":"R25","pred":"prep","subj":"T171","obj":"T170"},{"id":"R26","pred":"det","subj":"T172","obj":"T173"},{"id":"R27","pred":"pobj","subj":"T173","obj":"T171"},{"id":"R29","pred":"nmod","subj":"T175","obj":"T173"},{"id":"R30","pred":"nmod","subj":"T176","obj":"T175"},{"id":"R31","pred":"amod","subj":"T177","obj":"T175"},{"id":"R32","pred":"nmod","subj":"T178","obj":"T175"},{"id":"R36","pred":"punct","subj":"T182","obj":"T168"},{"id":"R37","pred":"det","subj":"T183","obj":"T184"},{"id":"R38","pred":"nsubj","subj":"T184","obj":"T168"},{"id":"R39","pred":"prep","subj":"T185","obj":"T184"},{"id":"R40","pred":"pobj","subj":"T186","obj":"T185"},{"id":"R41","pred":"advmod","subj":"T187","obj":"T188"},{"id":"R42","pred":"acomp","subj":"T188","obj":"T168"},{"id":"R20","pred":"amod","subj":"T165","obj":"T166"},{"id":"R21","pred":"nsubjpass","subj":"T166","obj":"T164"},{"id":"R22","pred":"auxpass","subj":"T167","obj":"T164"},{"id":"R28","pred":"amod","subj":"T174","obj":"T175"},{"id":"R33","pred":"punct","subj":"T179","obj":"T175"},{"id":"R34","pred":"appos","subj":"T180","obj":"T175"},{"id":"R35","pred":"punct","subj":"T181","obj":"T173"}],"text":" cystic fibrosis is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, the severity of disease is highly variable indicatin"}
craft-ca-core-ex-dev
{"project":"craft-ca-core-ex-dev","denotations":[{"id":"T79","span":{"begin":30,"end":39},"obj":"SO_EXT:sequence_alteration_entity_or_process"},{"id":"T80","span":{"begin":47,"end":98},"obj":"PR_EXT:000001044"},{"id":"T81","span":{"begin":63,"end":88},"obj":"GO:0055085"},{"id":"T82","span":{"begin":68,"end":76},"obj":"GO:0016020"},{"id":"T83","span":{"begin":89,"end":98},"obj":"GO_EXT:regulator"},{"id":"T84","span":{"begin":100,"end":104},"obj":"PR_EXT:000001044"},{"id":"T85","span":{"begin":106,"end":110},"obj":"SO_EXT:0000704"}],"text":" cystic fibrosis is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, the severity of disease is highly variable indicatin"}
craft-ca-core-dev
{"project":"craft-ca-core-dev","denotations":[{"id":"T37","span":{"begin":106,"end":110},"obj":"SO:0000704"},{"id":"T33","span":{"begin":47,"end":98},"obj":"PR:000001044"},{"id":"T34","span":{"begin":63,"end":88},"obj":"GO:0055085"},{"id":"T35","span":{"begin":68,"end":76},"obj":"GO:0016020"},{"id":"T36","span":{"begin":100,"end":104},"obj":"PR:000001044"}],"text":" cystic fibrosis is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, the severity of disease is highly variable indicatin"}