dgn-np:NP609861.RAyOXOyPr-BQhvlixX68wVr6Xli2LNkoY6JqBkqDj9wFY130_provenance {
  dgn-np:NP609861.RAyOXOyPr-BQhvlixX68wVr6Xli2LNkoY6JqBkqDj9wFY130_assertion dcterms:description "[Although recessive mutations in the anion transporter gene SLC26A4 are known to be responsible for Pendred syndrome (PS) and nonsyndromic hearing loss associated with enlarged vestibular aqueduct (EVA), also known as DFNB4, a large percentage of patients with this phenotype lack mutations in the SLC26A4 coding region in one or both alleles.]. 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:17503324 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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 .
}