@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP483421.RACYcDGbG41-rXbjlEWFHkB59TNcc1En59XnULh8TWMDg> .
@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:NP483421.RACYcDGbG41-rXbjlEWFHkB59TNcc1En59XnULh8TWMDg130_head {
  this: np:hasAssertion dgn-np:NP483421.RACYcDGbG41-rXbjlEWFHkB59TNcc1En59XnULh8TWMDg130_assertion;
    np:hasProvenance dgn-np:NP483421.RACYcDGbG41-rXbjlEWFHkB59TNcc1En59XnULh8TWMDg130_provenance;
    np:hasPublicationInfo dgn-np:NP483421.RACYcDGbG41-rXbjlEWFHkB59TNcc1En59XnULh8TWMDg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP483421.RACYcDGbG41-rXbjlEWFHkB59TNcc1En59XnULh8TWMDg130_assertion a np:Assertion .
  
  dgn-np:NP483421.RACYcDGbG41-rXbjlEWFHkB59TNcc1En59XnULh8TWMDg130_provenance a np:Provenance .
  
  dgn-np:NP483421.RACYcDGbG41-rXbjlEWFHkB59TNcc1En59XnULh8TWMDg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP483421.RACYcDGbG41-rXbjlEWFHkB59TNcc1En59XnULh8TWMDg130_assertion {
  miriam-gene:64072 a ncit:C16612 .
  
  lld:C0011053 a ncit:C7057 .
  
  dgn-gda:DGNb5adc4552ab12a1f0732d2a6b93bba12 sio:SIO_000628 miriam-gene:64072, lld:C0011053;
    a sio:SIO_001121 .
}

dgn-np:NP483421.RACYcDGbG41-rXbjlEWFHkB59TNcc1En59XnULh8TWMDg130_provenance {
  dgn-np:NP483421.RACYcDGbG41-rXbjlEWFHkB59TNcc1En59XnULh8TWMDg130_assertion dcterms:description
      "[Mutations in the human cadherin 23 (CDH23) gene cause deafness, neurosensory, autosomal recessive 12 (DFNB12) nonsyndromic hearing loss or Usher syndrome, type 1D (characterized by hearing impairment, vestibular dysfunction, and visual impairment).]. 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:21689626;
    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:NP483421.RACYcDGbG41-rXbjlEWFHkB59TNcc1En59XnULh8TWMDg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:49+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" .
}