@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP104497.RATL7W-WEU0WSN0Dg4JhtCsk0DZODT1AA7GhV3sgS4bUI> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP104497.RATL7W-WEU0WSN0Dg4JhtCsk0DZODT1AA7GhV3sgS4bUI130_head {
  this: np:hasAssertion dgn-np:NP104497.RATL7W-WEU0WSN0Dg4JhtCsk0DZODT1AA7GhV3sgS4bUI130_assertion;
    np:hasProvenance dgn-np:NP104497.RATL7W-WEU0WSN0Dg4JhtCsk0DZODT1AA7GhV3sgS4bUI130_provenance;
    np:hasPublicationInfo dgn-np:NP104497.RATL7W-WEU0WSN0Dg4JhtCsk0DZODT1AA7GhV3sgS4bUI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP104497.RATL7W-WEU0WSN0Dg4JhtCsk0DZODT1AA7GhV3sgS4bUI130_assertion a np:Assertion .
  
  dgn-np:NP104497.RATL7W-WEU0WSN0Dg4JhtCsk0DZODT1AA7GhV3sgS4bUI130_provenance a np:Provenance .
  
  dgn-np:NP104497.RATL7W-WEU0WSN0Dg4JhtCsk0DZODT1AA7GhV3sgS4bUI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP104497.RATL7W-WEU0WSN0Dg4JhtCsk0DZODT1AA7GhV3sgS4bUI130_assertion {
  miriam-gene:3014 a ncit:C16612 .
  
  lld:C0004509 a ncit:C7057 .
  
  dgn-gda:DGN5fff760ee516576bf1ed33d13612eced sio:SIO_000628 miriam-gene:3014, lld:C0004509;
    a sio:SIO_001122 .
}

dgn-np:NP104497.RATL7W-WEU0WSN0Dg4JhtCsk0DZODT1AA7GhV3sgS4bUI130_provenance {
  dgn-np:NP104497.RATL7W-WEU0WSN0Dg4JhtCsk0DZODT1AA7GhV3sgS4bUI130_assertion dcterms:description
      "[To investigate the possible association of variations of the H2AX gene with spermatogenic impairment in humans, mutation screening of the entire coding region of this gene was carried out in 302 patients with azoospermia or severe oligospermia along with 198 normospermic controls.]. 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:18536151;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP104497.RATL7W-WEU0WSN0Dg4JhtCsk0DZODT1AA7GhV3sgS4bUI130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:38+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}