@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP296863.RAP3gu3ZVLX9Tf_caVmwHWnmSVo80dII2YOQ9Zl3yaGKc> .
@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:NP296863.RAP3gu3ZVLX9Tf_caVmwHWnmSVo80dII2YOQ9Zl3yaGKc130_head {
  this: np:hasAssertion dgn-np:NP296863.RAP3gu3ZVLX9Tf_caVmwHWnmSVo80dII2YOQ9Zl3yaGKc130_assertion;
    np:hasProvenance dgn-np:NP296863.RAP3gu3ZVLX9Tf_caVmwHWnmSVo80dII2YOQ9Zl3yaGKc130_provenance;
    np:hasPublicationInfo dgn-np:NP296863.RAP3gu3ZVLX9Tf_caVmwHWnmSVo80dII2YOQ9Zl3yaGKc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP296863.RAP3gu3ZVLX9Tf_caVmwHWnmSVo80dII2YOQ9Zl3yaGKc130_assertion a np:Assertion .
  
  dgn-np:NP296863.RAP3gu3ZVLX9Tf_caVmwHWnmSVo80dII2YOQ9Zl3yaGKc130_provenance a np:Provenance .
  
  dgn-np:NP296863.RAP3gu3ZVLX9Tf_caVmwHWnmSVo80dII2YOQ9Zl3yaGKc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP296863.RAP3gu3ZVLX9Tf_caVmwHWnmSVo80dII2YOQ9Zl3yaGKc130_assertion {
  miriam-gene:100128922 a ncit:C16612 .
  
  lld:C0011053 a ncit:C7057 .
  
  dgn-gda:DGN26c3e33d829f96ac861be12eceb2fe3a sio:SIO_000628 miriam-gene:100128922,
      lld:C0011053;
    a sio:SIO_001121 .
}

dgn-np:NP296863.RAP3gu3ZVLX9Tf_caVmwHWnmSVo80dII2YOQ9Zl3yaGKc130_provenance {
  dgn-np:NP296863.RAP3gu3ZVLX9Tf_caVmwHWnmSVo80dII2YOQ9Zl3yaGKc130_assertion dcterms:description
      "[The possible implication of the mutation of the connexin gene in the pathophysiology of some progressive adult deafness opens new prospects in the fine diagnostic of the ear diseases and eventually may lead to new therapeutic strategies applied to the cochlea.]. 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:10928803;
    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:NP296863.RAP3gu3ZVLX9Tf_caVmwHWnmSVo80dII2YOQ9Zl3yaGKc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:48+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" .
}