PMC:1208879 / 189-297 JSONTXT

{"project":"craft-sa-dev","denotations":[{"id":"T209","span":{"begin":3,"end":4},"obj":"DT"},{"id":"T210","span":{"begin":9,"end":13},"obj":"NN"},{"id":"T211","span":{"begin":5,"end":8},"obj":"JJ"},{"id":"T212","span":{"begin":14,"end":16},"obj":"IN"},{"id":"T213","span":{"begin":17,"end":23},"obj":"JJ"},{"id":"T214","span":{"begin":41,"end":52},"obj":"NN"},{"id":"T215","span":{"begin":24,"end":27},"obj":"CC"},{"id":"T216","span":{"begin":28,"end":40},"obj":"JJ"},{"id":"T217","span":{"begin":52,"end":53},"obj":"."},{"id":"T219","span":{"begin":54,"end":65},"obj":"NNS"},{"id":"T221","span":{"begin":66,"end":70},"obj":"IN"},{"id":"T222","span":{"begin":71,"end":83},"obj":"JJ"},{"id":"T224","span":{"begin":84,"end":88},"obj":"NN"},{"id":"T225","span":{"begin":88,"end":89},"obj":"HYPH"},{"id":"T226","span":{"begin":89,"end":91},"obj":"IN"},{"id":"T227","span":{"begin":91,"end":92},"obj":"HYPH"},{"id":"T228","span":{"begin":92,"end":100},"obj":"NN"}],"relations":[{"id":"R30","pred":"amod","subj":"T211","obj":"T210"},{"id":"R33","pred":"pobj","subj":"T214","obj":"T212"},{"id":"R34","pred":"cc","subj":"T215","obj":"T213"},{"id":"R35","pred":"conj","subj":"T216","obj":"T213"},{"id":"R42","pred":"punct","subj":"T225","obj":"T224"},{"id":"R43","pred":"prep","subj":"T226","obj":"T224"},{"id":"R44","pred":"punct","subj":"T227","obj":"T226"},{"id":"R45","pred":"pobj","subj":"T228","obj":"T226"},{"id":"R28","pred":"det","subj":"T209","obj":"T210"},{"id":"R31","pred":"prep","subj":"T212","obj":"T210"},{"id":"R32","pred":"amod","subj":"T213","obj":"T214"},{"id":"R38","pred":"prep","subj":"T221","obj":"T219"}],"text":"th a key role in ocular and neurological development. Individuals with heterozygous loss-of-function mutatio"}

{"project":"craft-ca-core-ex-dev","denotations":[{"id":"T115","span":{"begin":17,"end":23},"obj":"UBERON:0000970"},{"id":"T116","span":{"begin":17,"end":23},"obj":"_FRAGMENT"},{"id":"T117","span":{"begin":41,"end":52},"obj":"GO:0001654"},{"id":"T118","span":{"begin":28,"end":40},"obj":"UBERON:0001016"},{"id":"T119","span":{"begin":28,"end":52},"obj":"GO:0007399"},{"id":"T120","span":{"begin":54,"end":65},"obj":"NCBITaxon:1"}],"relations":[{"id":"R1","pred":"_lexicallyChainedTo","subj":"T117","obj":"T116"}],"text":"th a key role in ocular and neurological development. Individuals with heterozygous loss-of-function mutatio"}

{"project":"craft-ca-core-dev","denotations":[{"id":"T67","span":{"begin":17,"end":23},"obj":"UBERON:0000970"},{"id":"T68","span":{"begin":17,"end":23},"obj":"_FRAGMENT"},{"id":"T69","span":{"begin":41,"end":52},"obj":"GO:0001654"},{"id":"T70","span":{"begin":28,"end":40},"obj":"UBERON:0001016"},{"id":"T71","span":{"begin":28,"end":52},"obj":"GO:0007399"},{"id":"T72","span":{"begin":54,"end":65},"obj":"NCBITaxon:1"}],"relations":[{"id":"R249","pred":"_lexicallyChainedTo","subj":"T69","obj":"T68"}],"text":"th a key role in ocular and neurological development. Individuals with heterozygous loss-of-function mutatio"}