PubMed:17273972 / 107-298 JSONTXT

{"project":"PMID_GLOBAL","denotations":[{"id":"T1","span":{"begin":0,"end":25},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":67,"end":75},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":162,"end":190},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"0008644"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"0002254"},{"id":"A3","pred":"mondo_id","subj":"T3","obj":"0008564"},{"id":"A4","pred":"mondo_id","subj":"T3","obj":"0008644"},{"id":"A5","pred":"mondo_id","subj":"T3","obj":"0018923"}],"text":"Deletion 22q11.2 syndrome is the most frequent known microdeletion syndrome and is associated with a highly variable phenotype, including DiGeorge and Shprintzen (velocardiofacial) syndromes."}

{"project":"TEST-DiseaseOrPhenotypicFeature","denotations":[{"id":"T2","span":{"begin":0,"end":25},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":162,"end":190},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A2","pred":"#label","subj":"T2","obj":"D004062"},{"id":"A3","pred":"#label","subj":"T3","obj":"D004062"}],"text":"Deletion 22q11.2 syndrome is the most frequent known microdeletion syndrome and is associated with a highly variable phenotype, including DiGeorge and Shprintzen (velocardiofacial) syndromes."}

{"project":"Test-merged","denotations":[{"id":"T3","span":{"begin":162,"end":190},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":0,"end":25},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A3","pred":"#label","subj":"T3","obj":"D004062"},{"id":"A2","pred":"#label","subj":"T2","obj":"D004062"}],"text":"Deletion 22q11.2 syndrome is the most frequent known microdeletion syndrome and is associated with a highly variable phenotype, including DiGeorge and Shprintzen (velocardiofacial) syndromes."}

{"project":"Test-merged-2","denotations":[{"id":"T2","span":{"begin":0,"end":25},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":162,"end":190},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A2","pred":"#label","subj":"T2","obj":"D004062"},{"id":"A3","pred":"#label","subj":"T3","obj":"D004062"}],"text":"Deletion 22q11.2 syndrome is the most frequent known microdeletion syndrome and is associated with a highly variable phenotype, including DiGeorge and Shprintzen (velocardiofacial) syndromes."}

{"project":"sentences","denotations":[{"id":"TextSentencer_T2","span":{"begin":0,"end":191},"obj":"Sentence"},{"id":"T2","span":{"begin":0,"end":191},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Deletion 22q11.2 syndrome is the most frequent known microdeletion syndrome and is associated with a highly variable phenotype, including DiGeorge and Shprintzen (velocardiofacial) syndromes."}

{"project":"PubCasesORDO","denotations":[{"id":"AB1","span":{"begin":163,"end":190},"obj":"ORDO:567"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":"Deletion 22q11.2 syndrome is the most frequent known microdeletion syndrome and is associated with a highly variable phenotype, including DiGeorge and Shprintzen (velocardiofacial) syndromes."}