@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP660928.RAdRA5fsl50r1QWZBmkRuBUTi2Wu4jrAgXU8DHdjXss5M> .
@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:NP660928.RAdRA5fsl50r1QWZBmkRuBUTi2Wu4jrAgXU8DHdjXss5M130_head {
  this: np:hasAssertion dgn-np:NP660928.RAdRA5fsl50r1QWZBmkRuBUTi2Wu4jrAgXU8DHdjXss5M130_assertion;
    np:hasProvenance dgn-np:NP660928.RAdRA5fsl50r1QWZBmkRuBUTi2Wu4jrAgXU8DHdjXss5M130_provenance;
    np:hasPublicationInfo dgn-np:NP660928.RAdRA5fsl50r1QWZBmkRuBUTi2Wu4jrAgXU8DHdjXss5M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP660928.RAdRA5fsl50r1QWZBmkRuBUTi2Wu4jrAgXU8DHdjXss5M130_assertion a np:Assertion .
  
  dgn-np:NP660928.RAdRA5fsl50r1QWZBmkRuBUTi2Wu4jrAgXU8DHdjXss5M130_provenance a np:Provenance .
  
  dgn-np:NP660928.RAdRA5fsl50r1QWZBmkRuBUTi2Wu4jrAgXU8DHdjXss5M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP660928.RAdRA5fsl50r1QWZBmkRuBUTi2Wu4jrAgXU8DHdjXss5M130_assertion {
  miriam-gene:7762 a ncit:C16612 .
  
  lld:C0010417 a ncit:C7057 .
  
  dgn-gda:DGNe837f1ed8dc7c909ef47764d82f3ee4f sio:SIO_000628 miriam-gene:7762, lld:C0010417;
    a sio:SIO_001121 .
}

dgn-np:NP660928.RAdRA5fsl50r1QWZBmkRuBUTi2Wu4jrAgXU8DHdjXss5M130_provenance {
  dgn-np:NP660928.RAdRA5fsl50r1QWZBmkRuBUTi2Wu4jrAgXU8DHdjXss5M130_assertion dcterms:description
      "[We hypothesized that the ZNF214 and ZNF215 genes, which are predominantly expressed in the testis, could be involved in male factor subfertility in patients with idiopathic impaired spermatogenesis or in patients with impaired spermatogenesis due to cryptorchidism.]. 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:12970396;
    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:NP660928.RAdRA5fsl50r1QWZBmkRuBUTi2Wu4jrAgXU8DHdjXss5M130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:39+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" .
}