PubMed:16440883 / 0-72 JSONTXT

{"project":"DisGeNET","denotations":[{"id":"T1","span":{"begin":0,"end":14},"obj":"disease:C0001193"},{"id":"T3","span":{"begin":20,"end":40},"obj":"disease:C0345354"}],"namespaces":[{"prefix":"gene","uri":"http://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"disease","uri":"http://purl.bioontology.org/ontology/MEDLINEPLUS/"}],"text":"Apert syndrome with preaxial polydactyly showing the typical mutation Se"}

{"project":"DisGeNET5_variant_disease","denotations":[{"id":"16440883-0#0#14#diseaseC0001193","span":{"begin":0,"end":14},"obj":"diseaseC0001193"}],"text":"Apert syndrome with preaxial polydactyly showing the typical mutation Se"}

{"project":"DisGeNET5_gene_disease","denotations":[{"id":"16440883-0#20#40#diseaseC0345354","span":{"begin":20,"end":40},"obj":"diseaseC0345354"}],"text":"Apert syndrome with preaxial polydactyly showing the typical mutation Se"}

{"project":"PubCasesHPO","denotations":[{"id":"TI1","span":{"begin":20,"end":40},"obj":"HP:0100258"}],"text":"Apert syndrome with preaxial polydactyly showing the typical mutation Se"}

{"project":"PubCasesORDO","denotations":[{"id":"TI1","span":{"begin":0,"end":14},"obj":"ORDO:87"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":"Apert syndrome with preaxial polydactyly showing the typical mutation Se"}