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<http://identifiers.org/ensembl/ENSG00000169057> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C16612> <http://purl.org/np/RAlSxnWHyMawH8dbQmdY9Xf3wI3I1LtNGAFDetWMirJrA#assertion> .
<http://identifiers.org/ensembl/ENSG00000169057> <http://www.w3.org/2000/01/rdf-schema#label> "MECP2" <http://purl.org/np/RAlSxnWHyMawH8dbQmdY9Xf3wI3I1LtNGAFDetWMirJrA#assertion> .
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<http://identifiers.org/pubmed/15689435> <http://purl.org/dc/terms/title> "Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndrome." <http://purl.org/np/RAlSxnWHyMawH8dbQmdY9Xf3wI3I1LtNGAFDetWMirJrA#provenance> .
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