@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP676348.RAXTUcbLTwEulk406dGCmnNPeCybouMoLwb15zON-YVhc> .
@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:NP676348.RAXTUcbLTwEulk406dGCmnNPeCybouMoLwb15zON-YVhc130_head {
  this: np:hasAssertion dgn-np:NP676348.RAXTUcbLTwEulk406dGCmnNPeCybouMoLwb15zON-YVhc130_assertion;
    np:hasProvenance dgn-np:NP676348.RAXTUcbLTwEulk406dGCmnNPeCybouMoLwb15zON-YVhc130_provenance;
    np:hasPublicationInfo dgn-np:NP676348.RAXTUcbLTwEulk406dGCmnNPeCybouMoLwb15zON-YVhc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP676348.RAXTUcbLTwEulk406dGCmnNPeCybouMoLwb15zON-YVhc130_assertion a np:Assertion .
  
  dgn-np:NP676348.RAXTUcbLTwEulk406dGCmnNPeCybouMoLwb15zON-YVhc130_provenance a np:Provenance .
  
  dgn-np:NP676348.RAXTUcbLTwEulk406dGCmnNPeCybouMoLwb15zON-YVhc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP676348.RAXTUcbLTwEulk406dGCmnNPeCybouMoLwb15zON-YVhc130_assertion {
  miriam-gene:10804 a ncit:C16612 .
  
  lld:C0018784 a ncit:C7057 .
  
  dgn-gda:DGN9b3408a6abfbedfd99d5c3070b115001 sio:SIO_000628 miriam-gene:10804, lld:C0018784;
    a sio:SIO_001121 .
}

dgn-np:NP676348.RAXTUcbLTwEulk406dGCmnNPeCybouMoLwb15zON-YVhc130_provenance {
  dgn-np:NP676348.RAXTUcbLTwEulk406dGCmnNPeCybouMoLwb15zON-YVhc130_assertion dcterms:description
      "[Genetic and auditory studies of 731 children with severe-to-profound hearing loss in US schools for the deaf and 46 additional children receiving clinical services for hearing loss ranging from moderate to profound demonstrated that mutations in the connexin 26 (GJB2) and connexin 30 (GJB6) genes explain at least 12% of those with nonsyndromic sensorineural 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:16222667;
    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:NP676348.RAXTUcbLTwEulk406dGCmnNPeCybouMoLwb15zON-YVhc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:48+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" .
}