clinvar.submission:
    alias: 
    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. Submissions for individual variation/phenotype combinations (SCV identifier) are also collected and made available separately. This collection references submissions, and is based on SCV accession.
    forward: http://www.ncbi.nlm.nih.gov/clinvar?term=${ac}
    institution: National Center for Biotechnology Information (NCBI), NIH, Maryland
    location: USA
    more: http://www.ncbi.nlm.nih.gov/clinvar/
    name: ClinVar Submission at NCBI
    pattern: ^SCV\d+(\.\d+)?$
    prefixed: false
    primary: false
    probe: http://www.ncbi.nlm.nih.gov/clinvar?term=SCV000151292
    provider: ncbi
    provider_id: MIR:00100795
    redirect: http://www.ncbi.nlm.nih.gov/clinvar?term=$id
    sort_score: 5
    state: 99:Up
    subject: 
    synonym: Global Research Identifier Database
    test: SCV000151292
    type: scheme

ncbi/clinvar.submission:
    for: clinvar.submission
    type: synonym