| http://identifiers.org/pubm... | rdf:type | biopax3:PublicationXref | lld:biopax3 |
| http://identifiers.org/pubm... | biopax3:author | Yata J | lld:biopax3 |
| http://identifiers.org/pubm... | biopax3:author | Shimozawa K | lld:biopax3 |
| http://identifiers.org/pubm... | biopax3:author | Saisho S | lld:biopax3 |
| http://identifiers.org/pubm... | biopax3:author | Koyama S | lld:biopax3 |
| http://identifiers.org/pubm... | biopax3:author | Toyoura T | lld:biopax3 |
| http://identifiers.org/pubm... | biopax3:db | PubMed | lld:biopax3 |
| http://identifiers.org/pubm... | biopax3:id | 12050231 | lld:biopax3 |
| http://identifiers.org/pubm... | biopax3:source | J Clin Endocrinol Metab 87(6);2668-73 | lld:biopax3 |
| http://identifiers.org/pubm... | biopax3:title | Genetic analysis of Japanese patients with 21-hydroxylase deficiency: identification of a patient with a new mutation of a homozygous deletion of adenine at codon 246 and patients without demonstrable mutations within the structural gene for CYP21. | lld:biopax3 |
| http://identifiers.org/pubm... | biopax3:year | 2002 | lld:biopax3 |
| http://biocyc.org/biopax/bi... | biopax3:xref | http://identifiers.org/pubm... | lld:biopax3 |
