
PMC:1186732 / 3392-3579
Annnotations
craft-sa-dev
{"project":"craft-sa-dev","denotations":[{"id":"T768","span":{"begin":0,"end":187},"obj":"sentence"},{"id":"T769","span":{"begin":1,"end":4},"obj":"DT"},{"id":"T770","span":{"begin":5,"end":12},"obj":"NN"},{"id":"T771","span":{"begin":16,"end":22},"obj":"VBN"},{"id":"T772","span":{"begin":13,"end":15},"obj":"VBZ"},{"id":"T773","span":{"begin":23,"end":25},"obj":"IN"},{"id":"T774","span":{"begin":26,"end":35},"obj":"NNS"},{"id":"T775","span":{"begin":36,"end":38},"obj":"IN"},{"id":"T776","span":{"begin":39,"end":42},"obj":"DT"},{"id":"T777","span":{"begin":81,"end":87},"obj":"NN"},{"id":"T778","span":{"begin":43,"end":49},"obj":"NN"},{"id":"T779","span":{"begin":58,"end":66},"obj":"NN"},{"id":"T780","span":{"begin":50,"end":57},"obj":"JJ"},{"id":"T781","span":{"begin":67,"end":80},"obj":"NN"},{"id":"T782","span":{"begin":88,"end":93},"obj":"NN"},{"id":"T783","span":{"begin":94,"end":95},"obj":"-LRB-"},{"id":"T784","span":{"begin":95,"end":99},"obj":"RB"},{"id":"T785","span":{"begin":100,"end":105},"obj":"VBN"},{"id":"T786","span":{"begin":106,"end":108},"obj":"IN"},{"id":"T787","span":{"begin":109,"end":122},"obj":"NN"},{"id":"T788","span":{"begin":131,"end":139},"obj":"NN"},{"id":"T789","span":{"begin":123,"end":130},"obj":"JJ"},{"id":"T790","span":{"begin":139,"end":140},"obj":"-RRB-"},{"id":"T791","span":{"begin":140,"end":142},"obj":","},{"id":"T792","span":{"begin":142,"end":147},"obj":"WDT"},{"id":"T793","span":{"begin":151,"end":160},"obj":"VBN"},{"id":"T794","span":{"begin":148,"end":150},"obj":"VBZ"},{"id":"T795","span":{"begin":161,"end":172},"obj":"RB"},{"id":"T796","span":{"begin":173,"end":175},"obj":"IN"},{"id":"T797","span":{"begin":176,"end":180},"obj":"NNS"},{"id":"T798","span":{"begin":181,"end":182},"obj":"-LRB-"},{"id":"T799","span":{"begin":184,"end":185},"obj":"CD"},{"id":"T800","span":{"begin":182,"end":183},"obj":"CD"},{"id":"T801","span":{"begin":183,"end":184},"obj":","},{"id":"T802","span":{"begin":185,"end":186},"obj":"-RRB-"},{"id":"T803","span":{"begin":186,"end":187},"obj":"."}],"relations":[{"id":"R357","pred":"det","subj":"T769","obj":"T770"},{"id":"R358","pred":"nsubjpass","subj":"T770","obj":"T771"},{"id":"R359","pred":"auxpass","subj":"T772","obj":"T771"},{"id":"R360","pred":"agent","subj":"T773","obj":"T771"},{"id":"R361","pred":"pobj","subj":"T774","obj":"T773"},{"id":"R362","pred":"prep","subj":"T775","obj":"T774"},{"id":"R363","pred":"det","subj":"T776","obj":"T777"},{"id":"R364","pred":"pobj","subj":"T777","obj":"T775"},{"id":"R365","pred":"nmod","subj":"T778","obj":"T779"},{"id":"R366","pred":"compound","subj":"T779","obj":"T777"},{"id":"R367","pred":"amod","subj":"T780","obj":"T779"},{"id":"R368","pred":"compound","subj":"T781","obj":"T777"},{"id":"R369","pred":"appos","subj":"T782","obj":"T777"},{"id":"R370","pred":"punct","subj":"T783","obj":"T777"},{"id":"R371","pred":"advmod","subj":"T784","obj":"T785"},{"id":"R372","pred":"acl","subj":"T785","obj":"T777"},{"id":"R373","pred":"prep","subj":"T786","obj":"T785"},{"id":"R374","pred":"nmod","subj":"T787","obj":"T788"},{"id":"R375","pred":"pobj","subj":"T788","obj":"T786"},{"id":"R376","pred":"amod","subj":"T789","obj":"T788"},{"id":"R377","pred":"punct","subj":"T790","obj":"T777"},{"id":"R378","pred":"punct","subj":"T791","obj":"T777"},{"id":"R379","pred":"dep","subj":"T792","obj":"T793"},{"id":"R380","pred":"relcl","subj":"T793","obj":"T777"},{"id":"R381","pred":"auxpass","subj":"T794","obj":"T793"},{"id":"R382","pred":"advmod","subj":"T795","obj":"T793"},{"id":"R383","pred":"prep","subj":"T796","obj":"T793"},{"id":"R384","pred":"pobj","subj":"T797","obj":"T796"},{"id":"R385","pred":"punct","subj":"T798","obj":"T799"},{"id":"R386","pred":"parataxis","subj":"T799","obj":"T771"},{"id":"R387","pred":"nummod","subj":"T800","obj":"T799"},{"id":"R388","pred":"punct","subj":"T801","obj":"T799"},{"id":"R389","pred":"punct","subj":"T802","obj":"T799"},{"id":"R390","pred":"punct","subj":"T803","obj":"T771"}],"text":" The disease is caused by mutations in the orphan nuclear receptor transcription factor NR2E3 (also known as photoreceptor nuclear receptor), which is expressed exclusively in rods [3,4]."}
craft-ca-core-ex-dev
{"project":"craft-ca-core-ex-dev","denotations":[{"id":"T624","span":{"begin":26,"end":35},"obj":"SO_EXT:sequence_alteration_entity_or_process"},{"id":"T625","span":{"begin":43,"end":49},"obj":"SO:0000910"},{"id":"T626","span":{"begin":50,"end":57},"obj":"GO:0005634"},{"id":"T627","span":{"begin":58,"end":66},"obj":"GO_EXT:0004872"},{"id":"T628","span":{"begin":67,"end":80},"obj":"GO_EXT:transcription"},{"id":"T629","span":{"begin":67,"end":87},"obj":"GO_EXT:transcription_factor"},{"id":"T630","span":{"begin":88,"end":93},"obj":"PR_EXT:000011403"},{"id":"T631","span":{"begin":109,"end":122},"obj":"CL:0000210"},{"id":"T632","span":{"begin":109,"end":139},"obj":"PR_EXT:000011403"},{"id":"T633","span":{"begin":123,"end":130},"obj":"GO:0005634"},{"id":"T634","span":{"begin":131,"end":139},"obj":"GO_EXT:0004872"},{"id":"T635","span":{"begin":151,"end":160},"obj":"GO:0010467"},{"id":"T636","span":{"begin":176,"end":180},"obj":"CL:0000604"}],"text":" The disease is caused by mutations in the orphan nuclear receptor transcription factor NR2E3 (also known as photoreceptor nuclear receptor), which is expressed exclusively in rods [3,4]."}
craft-ca-core-dev
{"project":"craft-ca-core-dev","denotations":[{"id":"T561","span":{"begin":43,"end":49},"obj":"SO:0000910"},{"id":"T562","span":{"begin":50,"end":57},"obj":"GO:0005634"},{"id":"T563","span":{"begin":88,"end":93},"obj":"PR:000011403"},{"id":"T564","span":{"begin":109,"end":122},"obj":"CL:0000210"},{"id":"T565","span":{"begin":109,"end":139},"obj":"PR:000011403"},{"id":"T566","span":{"begin":123,"end":130},"obj":"GO:0005634"},{"id":"T567","span":{"begin":151,"end":160},"obj":"GO:0010467"},{"id":"T568","span":{"begin":176,"end":180},"obj":"CL:0000604"}],"text":" The disease is caused by mutations in the orphan nuclear receptor transcription factor NR2E3 (also known as photoreceptor nuclear receptor), which is expressed exclusively in rods [3,4]."}
2_test
{"project":"2_test","denotations":[{"id":"16110338-10655056-85798500","span":{"begin":182,"end":183},"obj":"10655056"},{"id":"16110338-15277507-85798501","span":{"begin":184,"end":185},"obj":"15277507"},{"id":"T82344","span":{"begin":182,"end":183},"obj":"10655056"},{"id":"T22466","span":{"begin":184,"end":185},"obj":"15277507"}],"text":" The disease is caused by mutations in the orphan nuclear receptor transcription factor NR2E3 (also known as photoreceptor nuclear receptor), which is expressed exclusively in rods [3,4]."}