@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP472779.RA4cEKNmYBj62SOcy8v2THGpm1t-uuIU_PJE072qL3gw4> .
@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:NP472779.RA4cEKNmYBj62SOcy8v2THGpm1t-uuIU_PJE072qL3gw4130_head {
  this: np:hasAssertion dgn-np:NP472779.RA4cEKNmYBj62SOcy8v2THGpm1t-uuIU_PJE072qL3gw4130_assertion;
    np:hasProvenance dgn-np:NP472779.RA4cEKNmYBj62SOcy8v2THGpm1t-uuIU_PJE072qL3gw4130_provenance;
    np:hasPublicationInfo dgn-np:NP472779.RA4cEKNmYBj62SOcy8v2THGpm1t-uuIU_PJE072qL3gw4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP472779.RA4cEKNmYBj62SOcy8v2THGpm1t-uuIU_PJE072qL3gw4130_assertion a np:Assertion .
  
  dgn-np:NP472779.RA4cEKNmYBj62SOcy8v2THGpm1t-uuIU_PJE072qL3gw4130_provenance a np:Provenance .
  
  dgn-np:NP472779.RA4cEKNmYBj62SOcy8v2THGpm1t-uuIU_PJE072qL3gw4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP472779.RA4cEKNmYBj62SOcy8v2THGpm1t-uuIU_PJE072qL3gw4130_assertion {
  miriam-gene:79784 a ncit:C16612 .
  
  lld:C0848765 a ncit:C7057 .
  
  dgn-gda:DGNaf2dd9edab004af59411856fd547c3df sio:SIO_000628 miriam-gene:79784, lld:C0848765;
    a sio:SIO_001121 .
}

dgn-np:NP472779.RA4cEKNmYBj62SOcy8v2THGpm1t-uuIU_PJE072qL3gw4130_provenance {
  dgn-np:NP472779.RA4cEKNmYBj62SOcy8v2THGpm1t-uuIU_PJE072qL3gw4130_assertion dcterms:description
      "[Within the refined DFNA4 interval the public databases list more than 50 genes, from which several appear to be promising DFNA4 candidates due to similarities with animal models and with other causative genes involved in hearing disability.]. 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:15042303;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP472779.RA4cEKNmYBj62SOcy8v2THGpm1t-uuIU_PJE072qL3gw4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:43+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>,
      <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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}