mappings:
  miriam: clinvar.submitter
miriam:
  deprecated: false
  description: ClinVar archives reports of relationships among medically important
    variants and phenotypes. It records human variation, interpretations of the relationship
    specific variations to human health, and supporting evidence for each interpretation.
    Each ClinVar record (RCV identifier) represents an aggregated view of interpretations
    of the same variation and condition from one or more submitters (Submitter IDs).
    Submissions for individual variation/phenotype combinations (SCV identifier) are
    also collected and made available separately. This collection references submitters
    (submitter ids) that submit the submissions (SCVs).
  homepage: https://www.ncbi.nlm.nih.gov/clinvar/
  id: 00000769
  name: ClinVar Submitter
  namespaceEmbeddedInLui: false
  pattern: ^\d+$
  prefix: clinvar.submitter
  sampleId: '26957'
  uri_format: https://www.ncbi.nlm.nih.gov/clinvar/submitters/$1