Source:http://linkedlifedata.com/resource/lhgdn/association:17275
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:17275 | lhgdn:found_in | pubmed-article:15557528 | lld:lhgdn |
| lhgdn:association:17275 | lhgdn:geneRifSource | An 806delG mutation of MECP2 was found in a boy with severe developmental delay, seizures, microcephaly, breathing dysfunction, and spontaneous and evoked myoclonic jerks of upper limbs. | lld:lhgdn |
| lhgdn:association:17275 | lhgdn:mesh_code | D008831 | lld:lhgdn |
| lhgdn:association:17275 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
| lhgdn:association:17275 | lhgdn:umls_code | umls-concept:C1956147 | lld:mappings |
| entrez-gene:4204 | lhgdn:associationId | lhgdn:association:17275 | lld:lhgdn |