PubMed:263442 / 442-765 JSONTXT

{"project":"sentences","denotations":[{"id":"TextSentencer_T4","span":{"begin":0,"end":323},"obj":"Sentence"},{"id":"T4","span":{"begin":0,"end":323},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Branchio-oto-renal dysplasia is an autosomal dominant disorder in which affected individuals may have preauricular pits, lachrymal duct stenosis, hearing loss, branchial fistulas or cysts, structural defects of the outer, middle, and inner ear, and renal anomalies, which may range from mild hypoplasia to complete absence."}

{"project":"PubmedHPO","denotations":[{"id":"T4","span":{"begin":13,"end":28},"obj":"HP_0000110"},{"id":"T5","span":{"begin":35,"end":53},"obj":"HP_0000006"},{"id":"T6","span":{"begin":102,"end":119},"obj":"HP_0004467"},{"id":"T7","span":{"begin":146,"end":158},"obj":"HP_0000365"},{"id":"T8","span":{"begin":160,"end":187},"obj":"HP_0009796"},{"id":"T9","span":{"begin":160,"end":178},"obj":"HP_0009795"},{"id":"T10","span":{"begin":249,"end":264},"obj":"HP_0012210"},{"id":"T11","span":{"begin":249,"end":264},"obj":"HP_0000077"}],"text":"Branchio-oto-renal dysplasia is an autosomal dominant disorder in which affected individuals may have preauricular pits, lachrymal duct stenosis, hearing loss, branchial fistulas or cysts, structural defects of the outer, middle, and inner ear, and renal anomalies, which may range from mild hypoplasia to complete absence."}

{"project":"performance-test","denotations":[{"id":"PD-UBERON-AE-B_T2","span":{"begin":240,"end":243},"obj":"http://purl.obolibrary.org/obo/UBERON_0001690"},{"id":"PD-UBERON-AE-B_T4","span":{"begin":115,"end":119},"obj":"http://purl.obolibrary.org/obo/UBERON_0016566"},{"id":"PD-UBERON-AE-B_T10","span":{"begin":131,"end":135},"obj":"http://purl.obolibrary.org/obo/UBERON_0000058"}],"text":"Branchio-oto-renal dysplasia is an autosomal dominant disorder in which affected individuals may have preauricular pits, lachrymal duct stenosis, hearing loss, branchial fistulas or cysts, structural defects of the outer, middle, and inner ear, and renal anomalies, which may range from mild hypoplasia to complete absence."}

{"project":"BioLarkPubmedHPO","denotations":[{"id":"HP:0000110","span":{"begin":13,"end":28},"obj":"HP:0000110"},{"id":"HP:0000006","span":{"begin":35,"end":53},"obj":"HP:0000006"},{"id":"HP:0004467","span":{"begin":102,"end":119},"obj":"HP:0004467"},{"id":"HP:0007925","span":{"begin":121,"end":144},"obj":"HP:0007925"},{"id":"HP:0000365","span":{"begin":146,"end":158},"obj":"HP:0000365"},{"id":"HP:0009795","span":{"begin":160,"end":178},"obj":"HP:0009795"},{"id":"HP:0009796","span":{"begin":160,"end":187},"obj":"HP:0009796"},{"id":"HP:0000359","span":{"begin":189,"end":243},"obj":"HP:0000359"},{"id":"HP:0000356","span":{"begin":189,"end":243},"obj":"HP:0000356"},{"id":"HP:0000370","span":{"begin":189,"end":243},"obj":"HP:0000370"},{"id":"HP:0000598","span":{"begin":189,"end":243},"obj":"HP:0000598"},{"id":"HP:0000077","span":{"begin":249,"end":264},"obj":"HP:0000077"},{"id":"T3","span":{"begin":13,"end":28},"obj":"HP:0000110"},{"id":"T4","span":{"begin":35,"end":53},"obj":"HP:0000006"},{"id":"T5","span":{"begin":102,"end":119},"obj":"HP:0004467"},{"id":"T6","span":{"begin":121,"end":144},"obj":"HP:0007925"},{"id":"T7","span":{"begin":146,"end":158},"obj":"HP:0000365"},{"id":"T8","span":{"begin":160,"end":178},"obj":"HP:0009795"},{"id":"T9","span":{"begin":160,"end":187},"obj":"HP:0009796"},{"id":"T10","span":{"begin":189,"end":243},"obj":"HP:0000359"},{"id":"T11","span":{"begin":189,"end":243},"obj":"HP:0000356"},{"id":"T12","span":{"begin":189,"end":243},"obj":"HP:0000370"},{"id":"T13","span":{"begin":189,"end":243},"obj":"HP:0000598"},{"id":"T14","span":{"begin":249,"end":264},"obj":"HP:0000077"},{"id":"T3","span":{"begin":13,"end":28},"obj":"HP:0000110"},{"id":"T4","span":{"begin":35,"end":53},"obj":"HP:0000006"},{"id":"T5","span":{"begin":102,"end":119},"obj":"HP:0004467"},{"id":"T6","span":{"begin":121,"end":144},"obj":"HP:0007925"},{"id":"T7","span":{"begin":146,"end":158},"obj":"HP:0000365"},{"id":"T8","span":{"begin":160,"end":178},"obj":"HP:0009795"},{"id":"T9","span":{"begin":160,"end":187},"obj":"HP:0009796"},{"id":"T10","span":{"begin":189,"end":243},"obj":"HP:0000359"},{"id":"T11","span":{"begin":189,"end":243},"obj":"HP:0000356"},{"id":"T12","span":{"begin":189,"end":243},"obj":"HP:0000370"},{"id":"T13","span":{"begin":189,"end":243},"obj":"HP:0000598"},{"id":"T14","span":{"begin":249,"end":264},"obj":"HP:0000077"},{"id":"T3","span":{"begin":13,"end":28},"obj":"HP:0000110"},{"id":"T4","span":{"begin":35,"end":53},"obj":"HP:0000006"},{"id":"T5","span":{"begin":102,"end":119},"obj":"HP:0004467"},{"id":"T6","span":{"begin":121,"end":144},"obj":"HP:0007925"},{"id":"T7","span":{"begin":146,"end":158},"obj":"HP:0000365"},{"id":"T8","span":{"begin":160,"end":178},"obj":"HP:0009795"},{"id":"T9","span":{"begin":160,"end":187},"obj":"HP:0009796"},{"id":"T10","span":{"begin":189,"end":243},"obj":"HP:0000359"},{"id":"T11","span":{"begin":189,"end":243},"obj":"HP:0000356"},{"id":"T12","span":{"begin":189,"end":243},"obj":"HP:0000370"},{"id":"T13","span":{"begin":189,"end":243},"obj":"HP:0000598"},{"id":"T14","span":{"begin":249,"end":264},"obj":"HP:0000077"}],"namespaces":[{"prefix":"HP:","uri":"http://compbio.charite.de/hpoweb/showterm?id=HP:"}],"text":"Branchio-oto-renal dysplasia is an autosomal dominant disorder in which affected individuals may have preauricular pits, lachrymal duct stenosis, hearing loss, branchial fistulas or cysts, structural defects of the outer, middle, and inner ear, and renal anomalies, which may range from mild hypoplasia to complete absence."}

{"project":"PubCasesHPO","denotations":[{"id":"AB2","span":{"begin":13,"end":28},"obj":"HP:0000110"},{"id":"AB3","span":{"begin":102,"end":119},"obj":"HP:0004467"},{"id":"AB4","span":{"begin":160,"end":178},"obj":"HP:0009795"}],"text":"Branchio-oto-renal dysplasia is an autosomal dominant disorder in which affected individuals may have preauricular pits, lachrymal duct stenosis, hearing loss, branchial fistulas or cysts, structural defects of the outer, middle, and inner ear, and renal anomalies, which may range from mild hypoplasia to complete absence."}

{"project":"UBERON-AE","denotations":[{"id":"PD-UBERON-AE-B_T2","span":{"begin":240,"end":243},"obj":"http://purl.obolibrary.org/obo/UBERON_0001690"},{"id":"PD-UBERON-AE-B_T4","span":{"begin":115,"end":119},"obj":"http://purl.obolibrary.org/obo/UBERON_0016566"},{"id":"PD-UBERON-AE-B_T10","span":{"begin":131,"end":135},"obj":"http://purl.obolibrary.org/obo/UBERON_0000058"}],"text":"Branchio-oto-renal dysplasia is an autosomal dominant disorder in which affected individuals may have preauricular pits, lachrymal duct stenosis, hearing loss, branchial fistulas or cysts, structural defects of the outer, middle, and inner ear, and renal anomalies, which may range from mild hypoplasia to complete absence."}

{"project":"PubCasesORDO","denotations":[{"id":"AB3","span":{"begin":13,"end":28},"obj":"ORDO:93108"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":"Branchio-oto-renal dysplasia is an autosomal dominant disorder in which affected individuals may have preauricular pits, lachrymal duct stenosis, hearing loss, branchial fistulas or cysts, structural defects of the outer, middle, and inner ear, and renal anomalies, which may range from mild hypoplasia to complete absence."}