@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP51520.RAez5HkF9OXGUm22XhCVveGluXdVxh0erPZqludPBG4zw> .
@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/v3.0.0/void/> .

dgn-np:NP51520.RAez5HkF9OXGUm22XhCVveGluXdVxh0erPZqludPBG4zw130_head {
  this: np:hasAssertion dgn-np:NP51520.RAez5HkF9OXGUm22XhCVveGluXdVxh0erPZqludPBG4zw130_assertion;
    np:hasProvenance dgn-np:NP51520.RAez5HkF9OXGUm22XhCVveGluXdVxh0erPZqludPBG4zw130_provenance;
    np:hasPublicationInfo dgn-np:NP51520.RAez5HkF9OXGUm22XhCVveGluXdVxh0erPZqludPBG4zw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP51520.RAez5HkF9OXGUm22XhCVveGluXdVxh0erPZqludPBG4zw130_assertion a np:Assertion .
  
  dgn-np:NP51520.RAez5HkF9OXGUm22XhCVveGluXdVxh0erPZqludPBG4zw130_provenance a np:Provenance .
  
  dgn-np:NP51520.RAez5HkF9OXGUm22XhCVveGluXdVxh0erPZqludPBG4zw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP51520.RAez5HkF9OXGUm22XhCVveGluXdVxh0erPZqludPBG4zw130_assertion {
  miriam-gene:2706 a ncit:C16612 .
  
  lld:C0018784 a ncit:C7057 .
  
  dgn-gda:DGNf6456f6846ecc271942265844815690c sio:SIO_000628 miriam-gene:2706, lld:C0018784;
    a sio:SIO_001122 .
}

dgn-np:NP51520.RAez5HkF9OXGUm22XhCVveGluXdVxh0erPZqludPBG4zw130_provenance {
  dgn-np:NP51520.RAez5HkF9OXGUm22XhCVveGluXdVxh0erPZqludPBG4zw130_assertion dcterms:description
      "[Ethnicity should be considered when determining the optimal sequence of diagnostic testing for idiopathic congenital sensorineural hearing loss. Asian patients, in particular, should all be screened for mutations in GJB2, especially in the case of mild he]. 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:21042228;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP51520.RAez5HkF9OXGUm22XhCVveGluXdVxh0erPZqludPBG4zw130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:08+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}