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- Bb01335f2f26ea6087c14186464517a6c hasDbXref 0000-0002-0736-9199 @default.
- Bb01335f2f26ea6087c14186464517a6c hasDbXref "PMID:28638495" @default.
- Bb01335f2f26ea6087c14186464517a6c type Axiom @default.
- Bb01335f2f26ea6087c14186464517a6c annotatedProperty IAO_0000115 @default.
- Bb01335f2f26ea6087c14186464517a6c annotatedSource HP_0010959 @default.
- Bb01335f2f26ea6087c14186464517a6c annotatedTarget "Congenital pulmonary airway malformation (CPAM) - previously known as congenital cystic adenomatoid malformation (CCAM) - is a relatively rare developmental malformation of the lower respiratory tract. It is a hamartomatous, dysplastic developmental abnormality of the lung characterized by abnormal airway patterning during lung branching morphogenesis and is formed by abnormal branching of the immature bronchioles." @default.