@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP63092.RArRmNq8jWVtBhirpo5RBr2CLfWov9qtpREDeUeNp0fCo> .
@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:NP63092.RArRmNq8jWVtBhirpo5RBr2CLfWov9qtpREDeUeNp0fCo130_head {
  this: np:hasAssertion dgn-np:NP63092.RArRmNq8jWVtBhirpo5RBr2CLfWov9qtpREDeUeNp0fCo130_assertion;
    np:hasProvenance dgn-np:NP63092.RArRmNq8jWVtBhirpo5RBr2CLfWov9qtpREDeUeNp0fCo130_provenance;
    np:hasPublicationInfo dgn-np:NP63092.RArRmNq8jWVtBhirpo5RBr2CLfWov9qtpREDeUeNp0fCo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP63092.RArRmNq8jWVtBhirpo5RBr2CLfWov9qtpREDeUeNp0fCo130_assertion a np:Assertion .
  
  dgn-np:NP63092.RArRmNq8jWVtBhirpo5RBr2CLfWov9qtpREDeUeNp0fCo130_provenance a np:Provenance .
  
  dgn-np:NP63092.RArRmNq8jWVtBhirpo5RBr2CLfWov9qtpREDeUeNp0fCo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP63092.RArRmNq8jWVtBhirpo5RBr2CLfWov9qtpREDeUeNp0fCo130_assertion {
  miriam-gene:9381 a ncit:C16612 .
  
  lld:C0018784 a ncit:C7057 .
  
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dgn-np:NP63092.RArRmNq8jWVtBhirpo5RBr2CLfWov9qtpREDeUeNp0fCo130_provenance {
  dgn-np:NP63092.RArRmNq8jWVtBhirpo5RBr2CLfWov9qtpREDeUeNp0fCo130_assertion dcterms:description
      "[The results of our study indicate that genetic diagnosis of subjects with auditory neuropathy and profound hearing impairment should be directed to the otoferlin gene. Our data are of concern to universal screening programs which use TEOAEs as the first detection test for hearing impairment in newborns, since this technique may overlook a nonnegligible proportion of cases.]. 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:14635104;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP63092.RArRmNq8jWVtBhirpo5RBr2CLfWov9qtpREDeUeNp0fCo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:30+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
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