Statements in which the resource exists.
SubjectPredicateObjectContext
lhgdn:association:53558lhgdn:found_inpubmed-article:16217032lld:lhgdn
lhgdn:association:53558lhgdn:geneRifSourceData 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:53558lhgdn:mesh_codeD008831lld:lhgdn
lhgdn:association:53558lhgdn:associationIdTypehttp://bio2rdf.org/euadr:Po...lld:lhgdn
lhgdn:association:53558lhgdn:umls_codeumls-concept:C1956147lld:mappings
entrez-gene:79648lhgdn:associationIdlhgdn:association:53558lld:lhgdn