Source:http://linkedlifedata.com/resource/lhgdn/association:3637
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:3637 | lhgdn:found_in | pubmed-article:17973689 | lld:lhgdn |
| lhgdn:association:3637 | lhgdn:geneRifSource | A novel missense mutation in the RUNT-domain (P210S) of RUNX2 was identified in 3 Japanese cleidocranial dysplasia siblings; they showed a wide variation in the number and position of supernumerary teeth | lld:lhgdn |
| lhgdn:association:3637 | lhgdn:mesh_code | D002973 | lld:lhgdn |
| lhgdn:association:3637 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
| lhgdn:association:3637 | lhgdn:umls_code | umls-concept:C0008928 | lld:mappings |
| entrez-gene:860 | lhgdn:associationId | lhgdn:association:3637 | lld:lhgdn |