PubMed:24123776 / 0-209
Annnotations
sentences
{"project":"sentences","denotations":[{"id":"TextSentencer_T1","span":{"begin":0,"end":127},"obj":"Sentence"},{"id":"T1","span":{"begin":0,"end":127},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Sensenbrenner syndrome (Cranioectodermal dysplasia): clinical and molecular analyses of 39 patients including two new patients.\nSensenbrenner syndrome, also known as cranioectodermal dysplasia, is a rare multi"}
PubCasesORDO
{"project":"PubCasesORDO","denotations":[{"id":"AB1","span":{"begin":128,"end":150},"obj":"ORDO:1515"},{"id":"TI1","span":{"begin":24,"end":50},"obj":"ORDO:1515"},{"id":"AB2","span":{"begin":166,"end":192},"obj":"ORDO:1515"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":"Sensenbrenner syndrome (Cranioectodermal dysplasia): clinical and molecular analyses of 39 patients including two new patients.\nSensenbrenner syndrome, also known as cranioectodermal dysplasia, is a rare multi"}