@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP164527.RAJEDwUVqL2U42Upn61orCzjlp4azKh9evOfQ0px27WQg> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP164527.RAJEDwUVqL2U42Upn61orCzjlp4azKh9evOfQ0px27WQg130_head {
  this: np:hasAssertion dgn-np:NP164527.RAJEDwUVqL2U42Upn61orCzjlp4azKh9evOfQ0px27WQg130_assertion;
    np:hasProvenance dgn-np:NP164527.RAJEDwUVqL2U42Upn61orCzjlp4azKh9evOfQ0px27WQg130_provenance;
    np:hasPublicationInfo dgn-np:NP164527.RAJEDwUVqL2U42Upn61orCzjlp4azKh9evOfQ0px27WQg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP164527.RAJEDwUVqL2U42Upn61orCzjlp4azKh9evOfQ0px27WQg130_assertion a np:Assertion .
  
  dgn-np:NP164527.RAJEDwUVqL2U42Upn61orCzjlp4azKh9evOfQ0px27WQg130_provenance a np:Provenance .
  
  dgn-np:NP164527.RAJEDwUVqL2U42Upn61orCzjlp4azKh9evOfQ0px27WQg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP164527.RAJEDwUVqL2U42Upn61orCzjlp4azKh9evOfQ0px27WQg130_assertion {
  miriam-gene:2706 a ncit:C16612 .
  
  lld:C0011053 a ncit:C7057 .
  
  dgn-gda:DGNf32bf0b159aace6ddbfae53c357e0408 sio:SIO_000628 miriam-gene:2706, lld:C0011053;
    a sio:SIO_001121 .
}

dgn-np:NP164527.RAJEDwUVqL2U42Upn61orCzjlp4azKh9evOfQ0px27WQg130_provenance {
  dgn-np:NP164527.RAJEDwUVqL2U42Upn61orCzjlp4azKh9evOfQ0px27WQg130_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-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 .
}

dgn-np:NP164527.RAJEDwUVqL2U42Upn61orCzjlp4azKh9evOfQ0px27WQg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:29+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}