@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1061745.RAn26ZzaJQOfA2FYlECl5uvOOcIvqa7BesVKjnxiUavnc> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1061745.RAn26ZzaJQOfA2FYlECl5uvOOcIvqa7BesVKjnxiUavnc130_head {
  this: np:hasAssertion dgn-np:NP1061745.RAn26ZzaJQOfA2FYlECl5uvOOcIvqa7BesVKjnxiUavnc130_assertion;
    np:hasProvenance dgn-np:NP1061745.RAn26ZzaJQOfA2FYlECl5uvOOcIvqa7BesVKjnxiUavnc130_provenance;
    np:hasPublicationInfo dgn-np:NP1061745.RAn26ZzaJQOfA2FYlECl5uvOOcIvqa7BesVKjnxiUavnc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1061745.RAn26ZzaJQOfA2FYlECl5uvOOcIvqa7BesVKjnxiUavnc130_assertion a np:Assertion .
  
  dgn-np:NP1061745.RAn26ZzaJQOfA2FYlECl5uvOOcIvqa7BesVKjnxiUavnc130_provenance a np:Provenance .
  
  dgn-np:NP1061745.RAn26ZzaJQOfA2FYlECl5uvOOcIvqa7BesVKjnxiUavnc130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1061745.RAn26ZzaJQOfA2FYlECl5uvOOcIvqa7BesVKjnxiUavnc130_assertion {
  miriam-gene:2706 a ncit:C16612 .
  
  lld:C3711374 a ncit:C7057 .
  
  dgn-gda:DGNa7abe4af421096559ee63880ebef0684 sio:SIO_000628 miriam-gene:2706, lld:C3711374;
    a sio:SIO_001122 .
}

dgn-np:NP1061745.RAn26ZzaJQOfA2FYlECl5uvOOcIvqa7BesVKjnxiUavnc130_provenance {
  dgn-np:NP1061745.RAn26ZzaJQOfA2FYlECl5uvOOcIvqa7BesVKjnxiUavnc130_assertion dcterms:description
      "[Our recent studies indicate that nonsyndromic hearing loss (NSHL) in the Saudi Arabian population is genetically heterogeneous and is not caused by mutations in GJB2 and GJB6, the most common genes for deafness in various populations worldwide.]. 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:23510777;
    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 .
}

dgn-np:NP1061745.RAn26ZzaJQOfA2FYlECl5uvOOcIvqa7BesVKjnxiUavnc130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:47+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetv3.0rdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}