PubMed:11278977 / 2081-2330 JSONTXT

{"project":"sentences","denotations":[{"id":"TextSentencer_T16","span":{"begin":0,"end":249},"obj":"Sentence"},{"id":"T16","span":{"begin":0,"end":249},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Unlike the genotype/phenotype relationship seen for type I collagen defects and osteogenesis imperfecta, the null allele in this family appears to cause clinical features similar to those seen in cases with structural alterations in type V collagen."}

{"project":"PubCasesORDO","denotations":[{"id":"AB1","span":{"begin":80,"end":103},"obj":"ORDO:666"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":"Unlike the genotype/phenotype relationship seen for type I collagen defects and osteogenesis imperfecta, the null allele in this family appears to cause clinical features similar to those seen in cases with structural alterations in type V collagen."}

{"project":"mondo_disease","denotations":[{"id":"T3","span":{"begin":80,"end":103},"obj":"Disease"}],"attributes":[{"id":"A3","pred":"mondo_id","subj":"T3","obj":"http://purl.obolibrary.org/obo/MONDO_0019019"}],"text":"Unlike the genotype/phenotype relationship seen for type I collagen defects and osteogenesis imperfecta, the null allele in this family appears to cause clinical features similar to those seen in cases with structural alterations in type V collagen."}

{"project":"CL-cell","denotations":[{"id":"T10","span":{"begin":52,"end":58},"obj":"Cell"}],"attributes":[{"id":"A10","pred":"cl_id","subj":"T10","obj":"http://purl.obolibrary.org/obo/CL:0004120"},{"id":"A11","pred":"cl_id","subj":"T10","obj":"http://purl.obolibrary.org/obo/CL:0004138"}],"text":"Unlike the genotype/phenotype relationship seen for type I collagen defects and osteogenesis imperfecta, the null allele in this family appears to cause clinical features similar to those seen in cases with structural alterations in type V collagen."}