@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP68399.RAQqrgZPEqkqsnCs8b80lD_bTImaCCfdPevaA2vjLIIMA> .
@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:NP68399.RAQqrgZPEqkqsnCs8b80lD_bTImaCCfdPevaA2vjLIIMA130_head {
  this: np:hasAssertion dgn-np:NP68399.RAQqrgZPEqkqsnCs8b80lD_bTImaCCfdPevaA2vjLIIMA130_assertion;
    np:hasProvenance dgn-np:NP68399.RAQqrgZPEqkqsnCs8b80lD_bTImaCCfdPevaA2vjLIIMA130_provenance;
    np:hasPublicationInfo dgn-np:NP68399.RAQqrgZPEqkqsnCs8b80lD_bTImaCCfdPevaA2vjLIIMA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP68399.RAQqrgZPEqkqsnCs8b80lD_bTImaCCfdPevaA2vjLIIMA130_assertion a np:Assertion .
  
  dgn-np:NP68399.RAQqrgZPEqkqsnCs8b80lD_bTImaCCfdPevaA2vjLIIMA130_provenance a np:Provenance .
  
  dgn-np:NP68399.RAQqrgZPEqkqsnCs8b80lD_bTImaCCfdPevaA2vjLIIMA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP68399.RAQqrgZPEqkqsnCs8b80lD_bTImaCCfdPevaA2vjLIIMA130_assertion {
  miriam-gene:5172 a ncit:C16612 .
  
  lld:C0581883 a ncit:C7057 .
  
  dgn-gda:DGNa497952b456d338335c4ee9e6ebfdfdb sio:SIO_000628 miriam-gene:5172, lld:C0581883;
    a sio:SIO_001122 .
}

dgn-np:NP68399.RAQqrgZPEqkqsnCs8b80lD_bTImaCCfdPevaA2vjLIIMA130_provenance {
  dgn-np:NP68399.RAQqrgZPEqkqsnCs8b80lD_bTImaCCfdPevaA2vjLIIMA130_assertion dcterms:description
      "[This genetic epidemiological study demonstrated that 26.65% of the prelingual deafness in Northern Chinese patients can be detected at younger ages by genetic testing of three common hearing loss genes (GJB2, SLC26A4 and mtDNA A1555G), and thus, early intervention measures could be undertaken to help them in language acquisition.]. 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:18274916;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP68399.RAQqrgZPEqkqsnCs8b80lD_bTImaCCfdPevaA2vjLIIMA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:32+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" .
}