@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP684486.RAhnXTgh1PeRZ_9YCquS_-o7Ha_7PFXsoKUcGIM0QfdgM> .
@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:NP684486.RAhnXTgh1PeRZ_9YCquS_-o7Ha_7PFXsoKUcGIM0QfdgM130_head {
  this: np:hasAssertion dgn-np:NP684486.RAhnXTgh1PeRZ_9YCquS_-o7Ha_7PFXsoKUcGIM0QfdgM130_assertion;
    np:hasProvenance dgn-np:NP684486.RAhnXTgh1PeRZ_9YCquS_-o7Ha_7PFXsoKUcGIM0QfdgM130_provenance;
    np:hasPublicationInfo dgn-np:NP684486.RAhnXTgh1PeRZ_9YCquS_-o7Ha_7PFXsoKUcGIM0QfdgM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP684486.RAhnXTgh1PeRZ_9YCquS_-o7Ha_7PFXsoKUcGIM0QfdgM130_assertion a np:Assertion .
  
  dgn-np:NP684486.RAhnXTgh1PeRZ_9YCquS_-o7Ha_7PFXsoKUcGIM0QfdgM130_provenance a np:Provenance .
  
  dgn-np:NP684486.RAhnXTgh1PeRZ_9YCquS_-o7Ha_7PFXsoKUcGIM0QfdgM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP684486.RAhnXTgh1PeRZ_9YCquS_-o7Ha_7PFXsoKUcGIM0QfdgM130_assertion {
  miriam-gene:692222 a ncit:C16612 .
  
  lld:C0018784 a ncit:C7057 .
  
  dgn-gda:DGN58274caa390cd56c70d1d745ff01b89e sio:SIO_000628 miriam-gene:692222, lld:C0018784;
    a sio:SIO_001121 .
}

dgn-np:NP684486.RAhnXTgh1PeRZ_9YCquS_-o7Ha_7PFXsoKUcGIM0QfdgM130_provenance {
  dgn-np:NP684486.RAhnXTgh1PeRZ_9YCquS_-o7Ha_7PFXsoKUcGIM0QfdgM130_assertion dcterms: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:NP684486.RAhnXTgh1PeRZ_9YCquS_-o7Ha_7PFXsoKUcGIM0QfdgM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:56+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" .
}