<HashMap><database>EVA</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Vcf>ftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB110852/MS_orval_anonymized_clean.vcf.gz</Vcf><Vcf>ftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB110852/MS_orval_anonymized_clean.vcf.gz.csi</Vcf><Other>ftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB110852/MS_orval_anonymized_clean.vcf.csi</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><dataset_type>Exome Sequencing</dataset_type><omics_type>Genomics</omics_type><submitter>Clinical institute of genomic medicine</submitter><instrument_platform>Illumina HiSeq 2000</instrument_platform><species>Homo Sapiens</species><full_dataset_link>https://www.ebi.ac.uk/eva/?eva-study=PRJEB110852</full_dataset_link><repository>EVA</repository></additional><is_claimable>false</is_claimable><name>Exploring digenic causes for multiple sclerosis</name><description>Archived data for the study "Exploring digenic causes for multiple sclerosis"</description><dates><publication>2026-03-31</publication></dates><accession>PRJEB110852</accession><cross_references><TAXONOMY>9606</TAXONOMY></cross_references></HashMap>