@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP855166.RArqWB4JU_IUeKRp0x2H-3hENUJSQyXAwQnlPucq2uaxg> .
@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:NP855166.RArqWB4JU_IUeKRp0x2H-3hENUJSQyXAwQnlPucq2uaxg130_head {
  this: np:hasAssertion dgn-np:NP855166.RArqWB4JU_IUeKRp0x2H-3hENUJSQyXAwQnlPucq2uaxg130_assertion;
    np:hasProvenance dgn-np:NP855166.RArqWB4JU_IUeKRp0x2H-3hENUJSQyXAwQnlPucq2uaxg130_provenance;
    np:hasPublicationInfo dgn-np:NP855166.RArqWB4JU_IUeKRp0x2H-3hENUJSQyXAwQnlPucq2uaxg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP855166.RArqWB4JU_IUeKRp0x2H-3hENUJSQyXAwQnlPucq2uaxg130_assertion a np:Assertion .
  
  dgn-np:NP855166.RArqWB4JU_IUeKRp0x2H-3hENUJSQyXAwQnlPucq2uaxg130_provenance a np:Provenance .
  
  dgn-np:NP855166.RArqWB4JU_IUeKRp0x2H-3hENUJSQyXAwQnlPucq2uaxg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP855166.RArqWB4JU_IUeKRp0x2H-3hENUJSQyXAwQnlPucq2uaxg130_assertion {
  miriam-gene:4790 a ncit:C16612 .
  
  lld:C0011053 a ncit:C7057 .
  
  dgn-gda:DGN6518f20e2684b21f0faf56dc67d48c42 sio:SIO_000628 miriam-gene:4790, lld:C0011053;
    a sio:SIO_001121 .
}

dgn-np:NP855166.RArqWB4JU_IUeKRp0x2H-3hENUJSQyXAwQnlPucq2uaxg130_provenance {
  dgn-np:NP855166.RArqWB4JU_IUeKRp0x2H-3hENUJSQyXAwQnlPucq2uaxg130_assertion dcterms:description
      "[To find the frequencies that were most affected by the genetic defect, the excess hearing loss of the 17 patients was calculated per frequency in comparison with the respective p50 and p95 thresholds of the normal population.]. 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:10993457;
    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:NP855166.RArqWB4JU_IUeKRp0x2H-3hENUJSQyXAwQnlPucq2uaxg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:43+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" .
}