@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP954503.RAK-7weH_3tH6fGHPPemsQhLQkBSC2yllTezAJVRLC0FI> .
@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/v3.0.0/void/> .

dgn-np:NP954503.RAK-7weH_3tH6fGHPPemsQhLQkBSC2yllTezAJVRLC0FI130_head {
  this: np:hasAssertion dgn-np:NP954503.RAK-7weH_3tH6fGHPPemsQhLQkBSC2yllTezAJVRLC0FI130_assertion;
    np:hasProvenance dgn-np:NP954503.RAK-7weH_3tH6fGHPPemsQhLQkBSC2yllTezAJVRLC0FI130_provenance;
    np:hasPublicationInfo dgn-np:NP954503.RAK-7weH_3tH6fGHPPemsQhLQkBSC2yllTezAJVRLC0FI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP954503.RAK-7weH_3tH6fGHPPemsQhLQkBSC2yllTezAJVRLC0FI130_assertion a np:Assertion .
  
  dgn-np:NP954503.RAK-7weH_3tH6fGHPPemsQhLQkBSC2yllTezAJVRLC0FI130_provenance a np:Provenance .
  
  dgn-np:NP954503.RAK-7weH_3tH6fGHPPemsQhLQkBSC2yllTezAJVRLC0FI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP954503.RAK-7weH_3tH6fGHPPemsQhLQkBSC2yllTezAJVRLC0FI130_assertion {
  miriam-gene:84059 a ncit:C16612 .
  
  lld:C0155552 a ncit:C7057 .
  
  dgn-gda:DGN963f6492e44ff847802a7a356e392822 sio:SIO_000628 miriam-gene:84059, lld:C0155552;
    a sio:SIO_001121 .
}

dgn-np:NP954503.RAK-7weH_3tH6fGHPPemsQhLQkBSC2yllTezAJVRLC0FI130_provenance {
  dgn-np:NP954503.RAK-7weH_3tH6fGHPPemsQhLQkBSC2yllTezAJVRLC0FI130_assertion dcterms:description
      "[Knock-out and mutation mouse models show that loss of Vlgr1 function leads to abnormal stereociliary development and hearing loss, indicating crucial roles of Vlgr1 in hearing transduction or auditory system development.]. 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:23180093;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP954503.RAK-7weH_3tH6fGHPPemsQhLQkBSC2yllTezAJVRLC0FI130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:23+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}