@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP626561.RAYQvmqN3lRx9WlcrMpv5_ffUGBRgtr0rPEehjCS1vU9U> .
@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:NP626561.RAYQvmqN3lRx9WlcrMpv5_ffUGBRgtr0rPEehjCS1vU9U130_head {
  this: np:hasAssertion dgn-np:NP626561.RAYQvmqN3lRx9WlcrMpv5_ffUGBRgtr0rPEehjCS1vU9U130_assertion;
    np:hasProvenance dgn-np:NP626561.RAYQvmqN3lRx9WlcrMpv5_ffUGBRgtr0rPEehjCS1vU9U130_provenance;
    np:hasPublicationInfo dgn-np:NP626561.RAYQvmqN3lRx9WlcrMpv5_ffUGBRgtr0rPEehjCS1vU9U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP626561.RAYQvmqN3lRx9WlcrMpv5_ffUGBRgtr0rPEehjCS1vU9U130_assertion a np:Assertion .
  
  dgn-np:NP626561.RAYQvmqN3lRx9WlcrMpv5_ffUGBRgtr0rPEehjCS1vU9U130_provenance a np:Provenance .
  
  dgn-np:NP626561.RAYQvmqN3lRx9WlcrMpv5_ffUGBRgtr0rPEehjCS1vU9U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP626561.RAYQvmqN3lRx9WlcrMpv5_ffUGBRgtr0rPEehjCS1vU9U130_assertion {
  miriam-gene:5172 a ncit:C16612 .
  
  lld:C0155552 a ncit:C7057 .
  
  dgn-gda:DGN933d73872a70d43d789b525c8a21f935 sio:SIO_000628 miriam-gene:5172, lld:C0155552;
    a sio:SIO_001121 .
}

dgn-np:NP626561.RAYQvmqN3lRx9WlcrMpv5_ffUGBRgtr0rPEehjCS1vU9U130_provenance {
  dgn-np:NP626561.RAYQvmqN3lRx9WlcrMpv5_ffUGBRgtr0rPEehjCS1vU9U130_assertion dcterms:description
      "[In this study, all the 21 exons of SLC26A4 were screened in 107 Chinese patients with hearing loss associated with EVA or both EVA and Mondini dysplasia (MD), taken from six multiplex and 95 simplex families.]. 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:17718863;
    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:NP626561.RAYQvmqN3lRx9WlcrMpv5_ffUGBRgtr0rPEehjCS1vU9U130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:29+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: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" .
}