PMC:1186732 / 509-674
Annnotations
craft-sa-dev
{"project":"craft-sa-dev","denotations":[{"id":"T264","span":{"begin":3,"end":6},"obj":"DT"},{"id":"T265","span":{"begin":29,"end":37},"obj":"NN"},{"id":"T266","span":{"begin":7,"end":12},"obj":"JJ"},{"id":"T267","span":{"begin":13,"end":21},"obj":"VBN"},{"id":"T268","span":{"begin":22,"end":23},"obj":"NN"},{"id":"T269","span":{"begin":24,"end":28},"obj":"NN"},{"id":"T270","span":{"begin":23,"end":24},"obj":"HYPH"},{"id":"T271","span":{"begin":38,"end":39},"obj":"-LRB-"},{"id":"T272","span":{"begin":39,"end":43},"obj":"NN"},{"id":"T273","span":{"begin":43,"end":44},"obj":"-RRB-"},{"id":"T274","span":{"begin":44,"end":45},"obj":"."},{"id":"T276","span":{"begin":46,"end":50},"obj":"DT"},{"id":"T277","span":{"begin":51,"end":57},"obj":"NN"},{"id":"T278","span":{"begin":58,"end":65},"obj":"VBZ"},{"id":"T279","span":{"begin":66,"end":67},"obj":"DT"},{"id":"T280","span":{"begin":80,"end":88},"obj":"NN"},{"id":"T281","span":{"begin":68,"end":79},"obj":"JJ"},{"id":"T282","span":{"begin":89,"end":91},"obj":"IN"},{"id":"T283","span":{"begin":92,"end":95},"obj":"DT"},{"id":"T284","span":{"begin":102,"end":110},"obj":"NN"},{"id":"T285","span":{"begin":96,"end":101},"obj":"NN"},{"id":"T286","span":{"begin":111,"end":113},"obj":"IN"},{"id":"T287","span":{"begin":114,"end":119},"obj":"NN"},{"id":"T288","span":{"begin":119,"end":121},"obj":","},{"id":"T289","span":{"begin":121,"end":123},"obj":"DT"},{"id":"T291","span":{"begin":124,"end":130},"obj":"NN"},{"id":"T292","span":{"begin":131,"end":138},"obj":"JJ"},{"id":"T293","span":{"begin":139,"end":147},"obj":"NN"},{"id":"T294","span":{"begin":148,"end":161},"obj":"NN"}],"relations":[{"id":"R80","pred":"det","subj":"T264","obj":"T265"},{"id":"R82","pred":"amod","subj":"T266","obj":"T265"},{"id":"R83","pred":"amod","subj":"T267","obj":"T265"},{"id":"R84","pred":"compound","subj":"T268","obj":"T269"},{"id":"R85","pred":"compound","subj":"T269","obj":"T265"},{"id":"R86","pred":"punct","subj":"T270","obj":"T269"},{"id":"R87","pred":"punct","subj":"T271","obj":"T265"},{"id":"R88","pred":"appos","subj":"T272","obj":"T265"},{"id":"R91","pred":"det","subj":"T276","obj":"T277"},{"id":"R92","pred":"nsubj","subj":"T277","obj":"T278"},{"id":"R93","pred":"det","subj":"T279","obj":"T280"},{"id":"R94","pred":"dobj","subj":"T280","obj":"T278"},{"id":"R95","pred":"amod","subj":"T281","obj":"T280"},{"id":"R96","pred":"prep","subj":"T282","obj":"T280"},{"id":"R97","pred":"det","subj":"T283","obj":"T284"},{"id":"R98","pred":"pobj","subj":"T284","obj":"T282"},{"id":"R99","pred":"compound","subj":"T285","obj":"T284"},{"id":"R100","pred":"prep","subj":"T286","obj":"T284"},{"id":"R101","pred":"pobj","subj":"T287","obj":"T286"},{"id":"R102","pred":"punct","subj":"T288","obj":"T287"},{"id":"R106","pred":"amod","subj":"T292","obj":"T293"}],"text":"or the human enhanced S-cone syndrome (ESCS). This mutant carries a spontaneous deletion in the mouse ortholog of NR2E3, an orphan nuclear receptor transcription fac"}
craft-ca-core-ex-dev
{"project":"craft-ca-core-ex-dev","denotations":[{"id":"T128","span":{"begin":7,"end":12},"obj":"NCBITaxon:9606"},{"id":"T129","span":{"begin":24,"end":28},"obj":"CL:0000573"},{"id":"T130","span":{"begin":51,"end":57},"obj":"SO_EXT:sequence_altered_entity"},{"id":"T131","span":{"begin":80,"end":88},"obj":"SO_EXT:sequence_deletion_entity_or_process"},{"id":"T132","span":{"begin":96,"end":101},"obj":"NCBITaxon:10088"},{"id":"T133","span":{"begin":102,"end":110},"obj":"SO_EXT:0000855"},{"id":"T134","span":{"begin":114,"end":119},"obj":"PR_EXT:000011403"},{"id":"T135","span":{"begin":124,"end":130},"obj":"SO:0000910"},{"id":"T136","span":{"begin":131,"end":138},"obj":"GO:0005634"},{"id":"T137","span":{"begin":139,"end":147},"obj":"GO_EXT:0004872"},{"id":"T138","span":{"begin":148,"end":161},"obj":"GO_EXT:transcription"}],"text":"or the human enhanced S-cone syndrome (ESCS). This mutant carries a spontaneous deletion in the mouse ortholog of NR2E3, an orphan nuclear receptor transcription fac"}
craft-ca-core-dev
{"project":"craft-ca-core-dev","denotations":[{"id":"T71","span":{"begin":7,"end":12},"obj":"NCBITaxon:9606"},{"id":"T72","span":{"begin":24,"end":28},"obj":"CL:0000573"},{"id":"T73","span":{"begin":96,"end":101},"obj":"NCBITaxon:10088"},{"id":"T74","span":{"begin":102,"end":110},"obj":"SO:0000855"},{"id":"T75","span":{"begin":114,"end":119},"obj":"PR:000011403"},{"id":"T76","span":{"begin":124,"end":130},"obj":"SO:0000910"},{"id":"T77","span":{"begin":131,"end":138},"obj":"GO:0005634"}],"text":"or the human enhanced S-cone syndrome (ESCS). This mutant carries a spontaneous deletion in the mouse ortholog of NR2E3, an orphan nuclear receptor transcription fac"}