Source:http://linkedlifedata.com/resource/lhgdn/association:16853
| Subject | Predicate | Object | Context |
|---|---|---|---|
| lhgdn:association:16853 | lhgdn:found_in | pubmed-article:16217032 | lld:lhgdn |
| lhgdn:association:16853 | lhgdn:geneRifSource | Data suggest that the microcephaly observed in patients with MCPH1 deficiencies is due to disruption of the ATR-BRCA1-Chk1 signaling pathway that is also disrupted in Seckel syndrome patients. | lld:lhgdn |
| lhgdn:association:16853 | lhgdn:mesh_code | D008831 | lld:lhgdn |
| lhgdn:association:16853 | lhgdn:associationIdType | http://bio2rdf.org/euadr:Po... | lld:lhgdn |
| lhgdn:association:16853 | lhgdn:umls_code | umls-concept:C1956147 | lld:mappings |
| entrez-gene:672 | lhgdn:associationId | lhgdn:association:16853 | lld:lhgdn |