@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP614893.RAuX7YzDPbSzCMUw1ZStXPpsc2oXM8kSHvUc_9iWh7chw> .
@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:NP614893.RAuX7YzDPbSzCMUw1ZStXPpsc2oXM8kSHvUc_9iWh7chw130_head {
  this: np:hasAssertion dgn-np:NP614893.RAuX7YzDPbSzCMUw1ZStXPpsc2oXM8kSHvUc_9iWh7chw130_assertion;
    np:hasProvenance dgn-np:NP614893.RAuX7YzDPbSzCMUw1ZStXPpsc2oXM8kSHvUc_9iWh7chw130_provenance;
    np:hasPublicationInfo dgn-np:NP614893.RAuX7YzDPbSzCMUw1ZStXPpsc2oXM8kSHvUc_9iWh7chw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP614893.RAuX7YzDPbSzCMUw1ZStXPpsc2oXM8kSHvUc_9iWh7chw130_assertion a np:Assertion .
  
  dgn-np:NP614893.RAuX7YzDPbSzCMUw1ZStXPpsc2oXM8kSHvUc_9iWh7chw130_provenance a np:Provenance .
  
  dgn-np:NP614893.RAuX7YzDPbSzCMUw1ZStXPpsc2oXM8kSHvUc_9iWh7chw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP614893.RAuX7YzDPbSzCMUw1ZStXPpsc2oXM8kSHvUc_9iWh7chw130_assertion {
  miriam-gene:5172 a ncit:C16612 .
  
  lld:C0018784 a ncit:C7057 .
  
  dgn-gda:DGN36e9a298a8f9ffc47409cfcd3419e584 sio:SIO_000628 miriam-gene:5172, lld:C0018784;
    a sio:SIO_001121 .
}

dgn-np:NP614893.RAuX7YzDPbSzCMUw1ZStXPpsc2oXM8kSHvUc_9iWh7chw130_provenance {
  dgn-np:NP614893.RAuX7YzDPbSzCMUw1ZStXPpsc2oXM8kSHvUc_9iWh7chw130_assertion dcterms:description
      "[This study aims to investigate the mutation spectrum of GJB2, mitochondrial 12S rRNA, and SLC26A4 genes of Han Chinese, Hui people, and Uyghur ethnicities in sensorineural hearing loss (SNHL) patients in northwest of China.]. 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:24804242;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP614893.RAuX7YzDPbSzCMUw1ZStXPpsc2oXM8kSHvUc_9iWh7chw130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:47+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}