@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP836344.RAITDO-QAVh5nHvt-TWgc4qqh69OT0b59le6l7AqToMkE> .
@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:NP836344.RAITDO-QAVh5nHvt-TWgc4qqh69OT0b59le6l7AqToMkE130_head {
  this: np:hasAssertion dgn-np:NP836344.RAITDO-QAVh5nHvt-TWgc4qqh69OT0b59le6l7AqToMkE130_assertion;
    np:hasProvenance dgn-np:NP836344.RAITDO-QAVh5nHvt-TWgc4qqh69OT0b59le6l7AqToMkE130_provenance;
    np:hasPublicationInfo dgn-np:NP836344.RAITDO-QAVh5nHvt-TWgc4qqh69OT0b59le6l7AqToMkE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP836344.RAITDO-QAVh5nHvt-TWgc4qqh69OT0b59le6l7AqToMkE130_assertion a np:Assertion .
  
  dgn-np:NP836344.RAITDO-QAVh5nHvt-TWgc4qqh69OT0b59le6l7AqToMkE130_provenance a np:Provenance .
  
  dgn-np:NP836344.RAITDO-QAVh5nHvt-TWgc4qqh69OT0b59le6l7AqToMkE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP836344.RAITDO-QAVh5nHvt-TWgc4qqh69OT0b59le6l7AqToMkE130_assertion {
  miriam-gene:2706 a ncit:C16612 .
  
  lld:C1852271 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP836344.RAITDO-QAVh5nHvt-TWgc4qqh69OT0b59le6l7AqToMkE130_provenance {
  dgn-np:NP836344.RAITDO-QAVh5nHvt-TWgc4qqh69OT0b59le6l7AqToMkE130_assertion dcterms:description
      "[Testing for individual genes associated with nonsyndromic hearing loss, beyond GJB2 which encodes Connexin 26, can become expensive and, without specific phenotypic features to guide selection of genes for testing (such as enlarged vestibular aqueducts, low frequency hearing loss or auditory neuropathy), it is not likely to yield an etiology.]. 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:21358183;
    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:NP836344.RAITDO-QAVh5nHvt-TWgc4qqh69OT0b59le6l7AqToMkE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:31+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}