| Predicate |
Object |
| contentType |
Journal Article |
| issn |
1432-1203 |
| issueIdentifier |
1 |
| pageRange |
112- |
| publicationName |
Human genetics |
| startingPage |
112 |
| bibliographicCitation |
Mueller OT, Coovadia A. Novel human pathological mutations. Gene symbol: MC2R. Disease: Glucocorticoid deficiency. Hum Genet. 2010 Jan;127(1):112. PMID: 20108423. |
| creator |
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_b74b1c57cee21b5e271088c65f1cf04d
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_0c41f238c466d27a57e279f8d0ee132c |
| date |
201001 |
| identifier |
https://pubmed.ncbi.nlm.nih.gov/20108423 |
| isPartOf |
https://portal.issn.org/resource/ISSN/1432-1203
http://rdf.ncbi.nlm.nih.gov/pubchem/journal/4137 |
| language |
English |
| source |
https://pubmed.ncbi.nlm.nih.gov/ |
| title |
Novel human pathological mutations. Gene symbol: MC2R. Disease: Glucocorticoid deficiency |
| discusses |
http://id.nlm.nih.gov/mesh/M0009322
http://id.nlm.nih.gov/mesh/M0221241
http://id.nlm.nih.gov/mesh/M0004703 |
| hasPrimarySubjectTerm |
http://id.nlm.nih.gov/mesh/D044103Q000235
http://id.nlm.nih.gov/mesh/D020125
http://id.nlm.nih.gov/mesh/D005938Q000172 |
| hasSubjectTerm |
http://id.nlm.nih.gov/mesh/D003062Q000235
http://id.nlm.nih.gov/mesh/D006801 |