@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP357558.RAAOMUrw7Ex4PcF1_zUdNzkS8MPKb_QrQGrytYugEDs4E> .
@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:NP357558.RAAOMUrw7Ex4PcF1_zUdNzkS8MPKb_QrQGrytYugEDs4E130_head {
  this: np:hasAssertion dgn-np:NP357558.RAAOMUrw7Ex4PcF1_zUdNzkS8MPKb_QrQGrytYugEDs4E130_assertion;
    np:hasProvenance dgn-np:NP357558.RAAOMUrw7Ex4PcF1_zUdNzkS8MPKb_QrQGrytYugEDs4E130_provenance;
    np:hasPublicationInfo dgn-np:NP357558.RAAOMUrw7Ex4PcF1_zUdNzkS8MPKb_QrQGrytYugEDs4E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP357558.RAAOMUrw7Ex4PcF1_zUdNzkS8MPKb_QrQGrytYugEDs4E130_assertion a np:Assertion .
  
  dgn-np:NP357558.RAAOMUrw7Ex4PcF1_zUdNzkS8MPKb_QrQGrytYugEDs4E130_provenance a np:Provenance .
  
  dgn-np:NP357558.RAAOMUrw7Ex4PcF1_zUdNzkS8MPKb_QrQGrytYugEDs4E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP357558.RAAOMUrw7Ex4PcF1_zUdNzkS8MPKb_QrQGrytYugEDs4E130_assertion {
  miriam-gene:80207 a ncit:C16612 .
  
  lld:C0029124 a ncit:C7057 .
  
  dgn-gda:DGN49b09fc98d6c1c1962abeb4cecf8b3d7 sio:SIO_000628 miriam-gene:80207, lld:C0029124;
    a sio:SIO_001121 .
}

dgn-np:NP357558.RAAOMUrw7Ex4PcF1_zUdNzkS8MPKb_QrQGrytYugEDs4E130_provenance {
  dgn-np:NP357558.RAAOMUrw7Ex4PcF1_zUdNzkS8MPKb_QrQGrytYugEDs4E130_assertion dct:description
      "[Linkage and sequence mutation analyses of the ADOA candidate genes OPA1, OPA3, OPA4, and OPA5, including the genes WFS1, GJB2, and GJB6 associated with recessive inherited OA or dominant LFSNHL, were performed.]. 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:16648378;
    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:NP357558.RAAOMUrw7Ex4PcF1_zUdNzkS8MPKb_QrQGrytYugEDs4E130_publicationInfo {
  this: dct:created "2014-10-02T12:35:29+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" .
}