@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP543079.RAhkKVhUHIJMObdE_l8uwua_WMLaxE1ZWgfFK2DPWcQxs> .
@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:NP543079.RAhkKVhUHIJMObdE_l8uwua_WMLaxE1ZWgfFK2DPWcQxs130_head {
  this: np:hasAssertion dgn-np:NP543079.RAhkKVhUHIJMObdE_l8uwua_WMLaxE1ZWgfFK2DPWcQxs130_assertion;
    np:hasProvenance dgn-np:NP543079.RAhkKVhUHIJMObdE_l8uwua_WMLaxE1ZWgfFK2DPWcQxs130_provenance;
    np:hasPublicationInfo dgn-np:NP543079.RAhkKVhUHIJMObdE_l8uwua_WMLaxE1ZWgfFK2DPWcQxs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP543079.RAhkKVhUHIJMObdE_l8uwua_WMLaxE1ZWgfFK2DPWcQxs130_assertion a np:Assertion .
  
  dgn-np:NP543079.RAhkKVhUHIJMObdE_l8uwua_WMLaxE1ZWgfFK2DPWcQxs130_provenance a np:Provenance .
  
  dgn-np:NP543079.RAhkKVhUHIJMObdE_l8uwua_WMLaxE1ZWgfFK2DPWcQxs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP543079.RAhkKVhUHIJMObdE_l8uwua_WMLaxE1ZWgfFK2DPWcQxs130_assertion {
  miriam-gene:619469 a ncit:C16612 .
  
  lld:C0028960 a ncit:C7057 .
  
  dgn-gda:DGN597c70361422ab514f1d32c8aa8595f1 sio:SIO_000628 miriam-gene:619469, lld:C0028960;
    a sio:SIO_001121 .
}

dgn-np:NP543079.RAhkKVhUHIJMObdE_l8uwua_WMLaxE1ZWgfFK2DPWcQxs130_provenance {
  dgn-np:NP543079.RAhkKVhUHIJMObdE_l8uwua_WMLaxE1ZWgfFK2DPWcQxs130_assertion dcterms:description
      "[Though a definitive genotype/phenotype correlation does not exist, large deletions spanning multiple AZF regions or microdeletions restricted to AZFa usually result in patients with Sertoli Cell Only (SCO) or severe oligozoospermia, whereas microdeletions restricted to AZFb or AZFc can result in patients with phenotypes which range from SCO to moderate oligozoospermia.]. 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:10230814;
    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:NP543079.RAhkKVhUHIJMObdE_l8uwua_WMLaxE1ZWgfFK2DPWcQxs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:27+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" .
}