Source:http://linkedlifedata.com/resource/lhgdn/association:13043
Subject | Predicate | Object | Context |
---|---|---|---|
lhgdn:association:13043 | lhgdn:found_in | pubmed-article:18405873 | lld:lhgdn |
lhgdn:association:13043 | lhgdn:geneRifSource | truncating mutations of DYRK1A result in a clinical phenotype including microcephaly. | lld:lhgdn |
lhgdn:association:13043 | lhgdn:mesh_code | D008831 | lld:lhgdn |
lhgdn:association:13043 | lhgdn:associationIdType | http://http://linkedlifedat... | lld:lhgdn |
lhgdn:association:13043 | lhgdn:umls_code | umls-concept:C1956147 | lld:mappings |
entrez-gene:1859 | lhgdn:associationId | lhgdn:association:13043 | lld:lhgdn |