@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP329436.RA5If364Df3c04fRj9WRQt5ljyUpf6ip3QPR4pdWPmZDk> .
@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:NP329436.RA5If364Df3c04fRj9WRQt5ljyUpf6ip3QPR4pdWPmZDk130_head {
  this: np:hasAssertion dgn-np:NP329436.RA5If364Df3c04fRj9WRQt5ljyUpf6ip3QPR4pdWPmZDk130_assertion;
    np:hasProvenance dgn-np:NP329436.RA5If364Df3c04fRj9WRQt5ljyUpf6ip3QPR4pdWPmZDk130_provenance;
    np:hasPublicationInfo dgn-np:NP329436.RA5If364Df3c04fRj9WRQt5ljyUpf6ip3QPR4pdWPmZDk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP329436.RA5If364Df3c04fRj9WRQt5ljyUpf6ip3QPR4pdWPmZDk130_assertion a np:Assertion .
  
  dgn-np:NP329436.RA5If364Df3c04fRj9WRQt5ljyUpf6ip3QPR4pdWPmZDk130_provenance a np:Provenance .
  
  dgn-np:NP329436.RA5If364Df3c04fRj9WRQt5ljyUpf6ip3QPR4pdWPmZDk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP329436.RA5If364Df3c04fRj9WRQt5ljyUpf6ip3QPR4pdWPmZDk130_assertion {
  miriam-gene:3342 a ncit:C16612 .
  
  lld:C0021364 a ncit:C7057 .
  
  dgn-gda:DGN72a7a40f9c8f2df5f31a6adabe2a31af sio:SIO_000628 miriam-gene:3342, lld:C0021364;
    a sio:SIO_001121 .
}

dgn-np:NP329436.RA5If364Df3c04fRj9WRQt5ljyUpf6ip3QPR4pdWPmZDk130_provenance {
  dgn-np:NP329436.RA5If364Df3c04fRj9WRQt5ljyUpf6ip3QPR4pdWPmZDk130_assertion dcterms:description
      "[Although we could not identify novel genetic regions specifically associated with male infertility, whole genome array CGH analysis with higher resolution including larger numbers of patients may be able to give an opportunity for identifying new genetic markers for male infertility.]. 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:22750321;
    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:NP329436.RA5If364Df3c04fRj9WRQt5ljyUpf6ip3QPR4pdWPmZDk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:14+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" .
}