@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP756766.RAoWPt_VhygZlG4D0spDV50lejaJku4QT3UjAcv7pDwBM> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP756766.RAoWPt_VhygZlG4D0spDV50lejaJku4QT3UjAcv7pDwBM130_head {
  this: np:hasAssertion dgn-np:NP756766.RAoWPt_VhygZlG4D0spDV50lejaJku4QT3UjAcv7pDwBM130_assertion;
    np:hasProvenance dgn-np:NP756766.RAoWPt_VhygZlG4D0spDV50lejaJku4QT3UjAcv7pDwBM130_provenance;
    np:hasPublicationInfo dgn-np:NP756766.RAoWPt_VhygZlG4D0spDV50lejaJku4QT3UjAcv7pDwBM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP756766.RAoWPt_VhygZlG4D0spDV50lejaJku4QT3UjAcv7pDwBM130_assertion a np:Assertion .
  
  dgn-np:NP756766.RAoWPt_VhygZlG4D0spDV50lejaJku4QT3UjAcv7pDwBM130_provenance a np:Provenance .
  
  dgn-np:NP756766.RAoWPt_VhygZlG4D0spDV50lejaJku4QT3UjAcv7pDwBM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP756766.RAoWPt_VhygZlG4D0spDV50lejaJku4QT3UjAcv7pDwBM130_assertion {
  miriam-gene:5456 a ncit:C16612 .
  
  lld:C0266589 a ncit:C7057 .
  
  dgn-gda:DGNc7bc8346b327c27a08dd90f8613561c9 sio:SIO_000628 miriam-gene:5456, lld:C0266589;
    a sio:SIO_001121 .
}

dgn-np:NP756766.RAoWPt_VhygZlG4D0spDV50lejaJku4QT3UjAcv7pDwBM130_provenance {
  dgn-np:NP756766.RAoWPt_VhygZlG4D0spDV50lejaJku4QT3UjAcv7pDwBM130_assertion dcterms:description
      "[Despite numerous reports on clinical evaluations and genetic analyses describing novel POU3F4 mutations, little is known about how such mutations affect normal functions of the POU3F4 protein and cause inner ear malformations and deafness.]. 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-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP756766.RAoWPt_VhygZlG4D0spDV50lejaJku4QT3UjAcv7pDwBM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:28+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}