PubMed:23528641 / 132-289 JSONTXT

{"project":"sentences","denotations":[{"id":"TextSentencer_T2","span":{"begin":0,"end":157},"obj":"Sentence"},{"id":"T2","span":{"begin":0,"end":157},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Pitt-Hopkins syndrome (PTHS) is a rare neurodevelopmental genetic disorder, remaining under-diagnosed due to similarities with other known genetic syndromes."}

{"project":"Allie","denotations":[{"id":"SS1_23528641_1_0","span":{"begin":0,"end":21},"obj":"expanded"},{"id":"SS2_23528641_1_0","span":{"begin":23,"end":27},"obj":"abbr"}],"relations":[{"id":"AE1_23528641_1_0","pred":"abbreviatedTo","subj":"SS1_23528641_1_0","obj":"SS2_23528641_1_0"}],"text":"Pitt-Hopkins syndrome (PTHS) is a rare neurodevelopmental genetic disorder, remaining under-diagnosed due to similarities with other known genetic syndromes."}

{"project":"PubCasesORDO","denotations":[{"id":"AB1","span":{"begin":0,"end":21},"obj":"ORDO:2896"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":"Pitt-Hopkins syndrome (PTHS) is a rare neurodevelopmental genetic disorder, remaining under-diagnosed due to similarities with other known genetic syndromes."}