dgn-np:NP485593.RAHT7EMTrBG6Y1mXNdEnm-FEDs_v72npfkx8H2nu9iBdQ130_provenance {
  dgn-np:NP485593.RAHT7EMTrBG6Y1mXNdEnm-FEDs_v72npfkx8H2nu9iBdQ130_assertion dcterms:description "[A systematic study of 42 Greek DMD/BMD families using 14 polymorphic markers that span the dystrophin gene was performed in order to assess the position and frequency of recombinants in the Greek population and to test whether `hot spots` of recombination and deletions coincide when exclusively studying DMD/BMD families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
    sio:SIO_000772 miriam-pubmed:7557964 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}