@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP304642.RAVSdLVcYFQ2N4KyElKpEAnCjJpWGy9L27XGsAkOm7Z5g> .
@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:NP304642.RAVSdLVcYFQ2N4KyElKpEAnCjJpWGy9L27XGsAkOm7Z5g130_head {
  this: np:hasAssertion dgn-np:NP304642.RAVSdLVcYFQ2N4KyElKpEAnCjJpWGy9L27XGsAkOm7Z5g130_assertion;
    np:hasProvenance dgn-np:NP304642.RAVSdLVcYFQ2N4KyElKpEAnCjJpWGy9L27XGsAkOm7Z5g130_provenance;
    np:hasPublicationInfo dgn-np:NP304642.RAVSdLVcYFQ2N4KyElKpEAnCjJpWGy9L27XGsAkOm7Z5g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP304642.RAVSdLVcYFQ2N4KyElKpEAnCjJpWGy9L27XGsAkOm7Z5g130_assertion a np:Assertion .
  
  dgn-np:NP304642.RAVSdLVcYFQ2N4KyElKpEAnCjJpWGy9L27XGsAkOm7Z5g130_provenance a np:Provenance .
  
  dgn-np:NP304642.RAVSdLVcYFQ2N4KyElKpEAnCjJpWGy9L27XGsAkOm7Z5g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP304642.RAVSdLVcYFQ2N4KyElKpEAnCjJpWGy9L27XGsAkOm7Z5g130_assertion {
  miriam-gene:5456 a ncit:C16612 .
  
  lld:C0011053 a ncit:C7057 .
  
  dgn-gda:DGNfa93c8c5062cd17b9ea4c8ae58de55df sio:SIO_000628 miriam-gene:5456, lld:C0011053;
    a sio:SIO_001121 .
}

dgn-np:NP304642.RAVSdLVcYFQ2N4KyElKpEAnCjJpWGy9L27XGsAkOm7Z5g130_provenance {
  dgn-np:NP304642.RAVSdLVcYFQ2N4KyElKpEAnCjJpWGy9L27XGsAkOm7Z5g130_assertion dcterms:description
      "[Since most of the mutations reported for DFN3 thus far are associated with regions that encode the DNA binding domains of POU3F4, our results strongly suggest that the deafness in DFN3 patients is largely due to the null function of POU3F4.]. 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:19671658;
    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:NP304642.RAVSdLVcYFQ2N4KyElKpEAnCjJpWGy9L27XGsAkOm7Z5g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:55+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" .
}