@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP458899.RAdh8StyF50hNlv_J5e_5xD-a2MxeZ57jJe3iM1X4ZDdw> .
@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:NP458899.RAdh8StyF50hNlv_J5e_5xD-a2MxeZ57jJe3iM1X4ZDdw130_head {
  this: np:hasAssertion dgn-np:NP458899.RAdh8StyF50hNlv_J5e_5xD-a2MxeZ57jJe3iM1X4ZDdw130_assertion;
    np:hasProvenance dgn-np:NP458899.RAdh8StyF50hNlv_J5e_5xD-a2MxeZ57jJe3iM1X4ZDdw130_provenance;
    np:hasPublicationInfo dgn-np:NP458899.RAdh8StyF50hNlv_J5e_5xD-a2MxeZ57jJe3iM1X4ZDdw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP458899.RAdh8StyF50hNlv_J5e_5xD-a2MxeZ57jJe3iM1X4ZDdw130_assertion a np:Assertion .
  
  dgn-np:NP458899.RAdh8StyF50hNlv_J5e_5xD-a2MxeZ57jJe3iM1X4ZDdw130_provenance a np:Provenance .
  
  dgn-np:NP458899.RAdh8StyF50hNlv_J5e_5xD-a2MxeZ57jJe3iM1X4ZDdw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP458899.RAdh8StyF50hNlv_J5e_5xD-a2MxeZ57jJe3iM1X4ZDdw130_assertion {
  miriam-gene:560 a ncit:C16612 .
  
  lld:C1861689 a ncit:C7057 .
  
  dgn-gda:DGN182eaf29ade6e9c31a3355aed95edfea sio:SIO_000628 miriam-gene:560, lld:C1861689;
    a sio:SIO_001121 .
}

dgn-np:NP458899.RAdh8StyF50hNlv_J5e_5xD-a2MxeZ57jJe3iM1X4ZDdw130_provenance {
  dgn-np:NP458899.RAdh8StyF50hNlv_J5e_5xD-a2MxeZ57jJe3iM1X4ZDdw130_assertion dcterms:description
      "[Because of conflicting results about the association between azoospermic patients with Klinefelter syndrome (KFS) and azoospermia factor (AZF) polymorphism, and because nothing is known about the association of KFS with partial AZFc deletions, an association study was performed in Tunisian KFS patients.]. 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:19909597;
    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:NP458899.RAdh8StyF50hNlv_J5e_5xD-a2MxeZ57jJe3iM1X4ZDdw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:33+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" .
}