@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP43570.RAiCIXg5PBsd_vjkcAUlROm4HztwcC3cpBNifDTt6Pt-c> .
@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 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:NP43570.RAiCIXg5PBsd_vjkcAUlROm4HztwcC3cpBNifDTt6Pt-c130_head {
  this: np:hasAssertion dgn-np:NP43570.RAiCIXg5PBsd_vjkcAUlROm4HztwcC3cpBNifDTt6Pt-c130_assertion;
    np:hasProvenance dgn-np:NP43570.RAiCIXg5PBsd_vjkcAUlROm4HztwcC3cpBNifDTt6Pt-c130_provenance;
    np:hasPublicationInfo dgn-np:NP43570.RAiCIXg5PBsd_vjkcAUlROm4HztwcC3cpBNifDTt6Pt-c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP43570.RAiCIXg5PBsd_vjkcAUlROm4HztwcC3cpBNifDTt6Pt-c130_assertion a np:Assertion .
  
  dgn-np:NP43570.RAiCIXg5PBsd_vjkcAUlROm4HztwcC3cpBNifDTt6Pt-c130_provenance a np:Provenance .
  
  dgn-np:NP43570.RAiCIXg5PBsd_vjkcAUlROm4HztwcC3cpBNifDTt6Pt-c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP43570.RAiCIXg5PBsd_vjkcAUlROm4HztwcC3cpBNifDTt6Pt-c130_assertion {
  miriam-gene:2706 a ncit:C16612 .
  
  lld:C0018784 a ncit:C7057 .
  
  dgn-gda:DGNc6061dc8d40383cd55266dec6722b37f sio:SIO_000628 miriam-gene:2706, lld:C0018784;
    a sio:SIO_001122 .
}

dgn-np:NP43570.RAiCIXg5PBsd_vjkcAUlROm4HztwcC3cpBNifDTt6Pt-c130_provenance {
  dgn-np:NP43570.RAiCIXg5PBsd_vjkcAUlROm4HztwcC3cpBNifDTt6Pt-c130_assertion dct:description
      "[Most probands have a congenital HL that is stable, symmetrical and without associated manifestations, but the audiometric profile should not be the only criteria for offering mutational screening of DFNB1 because of the observed variability.]. 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:18758381;
    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:NP43570.RAiCIXg5PBsd_vjkcAUlROm4HztwcC3cpBNifDTt6Pt-c130_publicationInfo {
  this: dct:created "2014-10-02T12:32:19+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}