PubMed:10482951 / 170-357 JSONTXT

{"project":"PubmedHPO","denotations":[{"id":"T1","span":{"begin":57,"end":82},"obj":"HP_0010864"},{"id":"T2","span":{"begin":64,"end":82},"obj":"HP_0001249"},{"id":"T3","span":{"begin":84,"end":106},"obj":"HP_0005484"},{"id":"T4","span":{"begin":94,"end":106},"obj":"HP_0000252"},{"id":"T5","span":{"begin":108,"end":119},"obj":"HP_0000154"},{"id":"T6","span":{"begin":124,"end":134},"obj":"HP_0000303"},{"id":"T7","span":{"begin":136,"end":153},"obj":"HP_0001344"},{"id":"T8","span":{"begin":155,"end":161},"obj":"HP_0001251"},{"id":"T9","span":{"begin":169,"end":186},"obj":"HP_0040082"}],"text":"The clinical features of Angelman syndrome (AS) comprise severe mental retardation, postnatal microcephaly, macrostomia and prognathia, absence of speech, ataxia, and a happy disposition."}

{"project":"BioLarkPubmedHPO","denotations":[{"id":"HP:0002187","span":{"begin":57,"end":82},"obj":"HP:0002187"},{"id":"HP:0005484","span":{"begin":84,"end":106},"obj":"HP:0005484"},{"id":"HP:0000181","span":{"begin":108,"end":119},"obj":"HP:0000181"},{"id":"HP:0000303","span":{"begin":124,"end":134},"obj":"HP:0000303"},{"id":"HP:0001617","span":{"begin":136,"end":153},"obj":"HP:0001617"},{"id":"HP:0001251","span":{"begin":155,"end":161},"obj":"HP:0001251"},{"id":"HP:0100024","span":{"begin":169,"end":186},"obj":"HP:0100024"},{"id":"T1","span":{"begin":57,"end":82},"obj":"HP:0002187"},{"id":"T2","span":{"begin":84,"end":106},"obj":"HP:0005484"},{"id":"T3","span":{"begin":108,"end":119},"obj":"HP:0000181"},{"id":"T4","span":{"begin":124,"end":134},"obj":"HP:0000303"},{"id":"T5","span":{"begin":136,"end":153},"obj":"HP:0001617"},{"id":"T6","span":{"begin":155,"end":161},"obj":"HP:0001251"},{"id":"T7","span":{"begin":169,"end":186},"obj":"HP:0100024"},{"id":"T1","span":{"begin":57,"end":82},"obj":"HP:0002187"},{"id":"T2","span":{"begin":84,"end":106},"obj":"HP:0005484"},{"id":"T3","span":{"begin":108,"end":119},"obj":"HP:0000181"},{"id":"T4","span":{"begin":124,"end":134},"obj":"HP:0000303"},{"id":"T5","span":{"begin":136,"end":153},"obj":"HP:0001617"},{"id":"T6","span":{"begin":155,"end":161},"obj":"HP:0001251"},{"id":"T7","span":{"begin":169,"end":186},"obj":"HP:0100024"},{"id":"T1","span":{"begin":57,"end":82},"obj":"HP:0002187"},{"id":"T2","span":{"begin":84,"end":106},"obj":"HP:0005484"},{"id":"T3","span":{"begin":108,"end":119},"obj":"HP:0000181"},{"id":"T4","span":{"begin":124,"end":134},"obj":"HP:0000303"},{"id":"T5","span":{"begin":136,"end":153},"obj":"HP:0001617"},{"id":"T6","span":{"begin":155,"end":161},"obj":"HP:0001251"},{"id":"T7","span":{"begin":169,"end":186},"obj":"HP:0100024"}],"namespaces":[{"prefix":"HP:","uri":"http://compbio.charite.de/hpoweb/showterm?id=HP:"}],"text":"The clinical features of Angelman syndrome (AS) comprise severe mental retardation, postnatal microcephaly, macrostomia and prognathia, absence of speech, ataxia, and a happy disposition."}

{"project":"PubCasesHPO","denotations":[{"id":"AB1","span":{"begin":84,"end":106},"obj":"HP:0005484"},{"id":"AB2","span":{"begin":155,"end":161},"obj":"HP:0001251"}],"text":"The clinical features of Angelman syndrome (AS) comprise severe mental retardation, postnatal microcephaly, macrostomia and prognathia, absence of speech, ataxia, and a happy disposition."}

{"project":"sentences","denotations":[{"id":"TextSentencer_T2","span":{"begin":0,"end":187},"obj":"Sentence"},{"id":"T2","span":{"begin":0,"end":187},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"The clinical features of Angelman syndrome (AS) comprise severe mental retardation, postnatal microcephaly, macrostomia and prognathia, absence of speech, ataxia, and a happy disposition."}

{"project":"PubCasesORDO","denotations":[{"id":"AB1","span":{"begin":25,"end":42},"obj":"ORDO:72"},{"id":"AB2","span":{"begin":108,"end":119},"obj":"ORDO:141276"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":"The clinical features of Angelman syndrome (AS) comprise severe mental retardation, postnatal microcephaly, macrostomia and prognathia, absence of speech, ataxia, and a happy disposition."}