@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP585559.RAW9DaPZPXhQL1-9wg6_BprhUnEf-sv4aDGWVLUt-slow> .
@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:NP585559.RAW9DaPZPXhQL1-9wg6_BprhUnEf-sv4aDGWVLUt-slow130_head {
  this: np:hasAssertion dgn-np:NP585559.RAW9DaPZPXhQL1-9wg6_BprhUnEf-sv4aDGWVLUt-slow130_assertion;
    np:hasProvenance dgn-np:NP585559.RAW9DaPZPXhQL1-9wg6_BprhUnEf-sv4aDGWVLUt-slow130_provenance;
    np:hasPublicationInfo dgn-np:NP585559.RAW9DaPZPXhQL1-9wg6_BprhUnEf-sv4aDGWVLUt-slow130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP585559.RAW9DaPZPXhQL1-9wg6_BprhUnEf-sv4aDGWVLUt-slow130_assertion a np:Assertion .
  
  dgn-np:NP585559.RAW9DaPZPXhQL1-9wg6_BprhUnEf-sv4aDGWVLUt-slow130_provenance a np:Provenance .
  
  dgn-np:NP585559.RAW9DaPZPXhQL1-9wg6_BprhUnEf-sv4aDGWVLUt-slow130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP585559.RAW9DaPZPXhQL1-9wg6_BprhUnEf-sv4aDGWVLUt-slow130_assertion {
  miriam-gene:100653377 a ncit:C16612 .
  
  lld:C0004509 a ncit:C7057 .
  
  dgn-gda:DGN34b6eb12cb6ef1c56807f87a91cedacb sio:SIO_000628 miriam-gene:100653377,
      lld:C0004509;
    a sio:SIO_001121 .
}

dgn-np:NP585559.RAW9DaPZPXhQL1-9wg6_BprhUnEf-sv4aDGWVLUt-slow130_provenance {
  dgn-np:NP585559.RAW9DaPZPXhQL1-9wg6_BprhUnEf-sv4aDGWVLUt-slow130_assertion dcterms:description
      "[In conclusion, chromosomal abnormality and AZF region microdeletion of Y chromosome might account for about 25% of Chinese infertile patients with azoospermia or severe oligozoospermia, suggesting the two abnormalities are important genetic etiology of spermatogenic failure in Chinese population and it is essential to screen them during diagnosis of male infertility before in vitro assisted fertilization by introcytoplasmic sperm injection.]. 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:16529294;
    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:NP585559.RAW9DaPZPXhQL1-9wg6_BprhUnEf-sv4aDGWVLUt-slow130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:52+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" .
}