@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1092125.RAnS0kquZWwP4mcmKxiymqZX40J0uw0KrZG6U7EXgA4vs> .
@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:NP1092125.RAnS0kquZWwP4mcmKxiymqZX40J0uw0KrZG6U7EXgA4vs130_head {
  this: np:hasAssertion dgn-np:NP1092125.RAnS0kquZWwP4mcmKxiymqZX40J0uw0KrZG6U7EXgA4vs130_assertion;
    np:hasProvenance dgn-np:NP1092125.RAnS0kquZWwP4mcmKxiymqZX40J0uw0KrZG6U7EXgA4vs130_provenance;
    np:hasPublicationInfo dgn-np:NP1092125.RAnS0kquZWwP4mcmKxiymqZX40J0uw0KrZG6U7EXgA4vs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1092125.RAnS0kquZWwP4mcmKxiymqZX40J0uw0KrZG6U7EXgA4vs130_assertion a np:Assertion .
  
  dgn-np:NP1092125.RAnS0kquZWwP4mcmKxiymqZX40J0uw0KrZG6U7EXgA4vs130_provenance a np:Provenance .
  
  dgn-np:NP1092125.RAnS0kquZWwP4mcmKxiymqZX40J0uw0KrZG6U7EXgA4vs130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1092125.RAnS0kquZWwP4mcmKxiymqZX40J0uw0KrZG6U7EXgA4vs130_assertion {
  miriam-gene:5172 a ncit:C16612 .
  
  lld:C3711374 a ncit:C7057 .
  
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}

dgn-np:NP1092125.RAnS0kquZWwP4mcmKxiymqZX40J0uw0KrZG6U7EXgA4vs130_provenance {
  dgn-np:NP1092125.RAnS0kquZWwP4mcmKxiymqZX40J0uw0KrZG6U7EXgA4vs130_assertion dcterms:description
      "[To analyze the prevalence of the three common deafness genes GJB2, mtDNA, and SLC26A4 gene mutations in Tibetan, Tu nationality, and Mongolian patients with nonsyndromic hearing impairment in the Northwest region of China.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    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:NP1092125.RAnS0kquZWwP4mcmKxiymqZX40J0uw0KrZG6U7EXgA4vs130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:01+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" .
}