@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP275566.RAXOhlowmHbLQo0i0cAxY1xORtBHPcXzH4N81P7CyazOA> .
@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:NP275566.RAXOhlowmHbLQo0i0cAxY1xORtBHPcXzH4N81P7CyazOA130_head {
  this: np:hasAssertion dgn-np:NP275566.RAXOhlowmHbLQo0i0cAxY1xORtBHPcXzH4N81P7CyazOA130_assertion;
    np:hasProvenance dgn-np:NP275566.RAXOhlowmHbLQo0i0cAxY1xORtBHPcXzH4N81P7CyazOA130_provenance;
    np:hasPublicationInfo dgn-np:NP275566.RAXOhlowmHbLQo0i0cAxY1xORtBHPcXzH4N81P7CyazOA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP275566.RAXOhlowmHbLQo0i0cAxY1xORtBHPcXzH4N81P7CyazOA130_assertion a np:Assertion .
  
  dgn-np:NP275566.RAXOhlowmHbLQo0i0cAxY1xORtBHPcXzH4N81P7CyazOA130_provenance a np:Provenance .
  
  dgn-np:NP275566.RAXOhlowmHbLQo0i0cAxY1xORtBHPcXzH4N81P7CyazOA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP275566.RAXOhlowmHbLQo0i0cAxY1xORtBHPcXzH4N81P7CyazOA130_assertion {
  miriam-gene:83983 a ncit:C16612 .
  
  lld:C0004509 a ncit:C7057 .
  
  dgn-gda:DGN99596a657494bfbebad785032523ef5c sio:SIO_000628 miriam-gene:83983, lld:C0004509;
    a sio:SIO_001121 .
}

dgn-np:NP275566.RAXOhlowmHbLQo0i0cAxY1xORtBHPcXzH4N81P7CyazOA130_provenance {
  dgn-np:NP275566.RAXOhlowmHbLQo0i0cAxY1xORtBHPcXzH4N81P7CyazOA130_assertion dcterms:description
      "[In order to investigate the possible relationships between variations, including mutations and polymorphisms of the TSSK4 gene and impaired spermatogenesis in humans, mutation screening of this gene in 372 patients with azoospermia or severe oligospermia and 220 controls was performed.]. 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:18390560;
    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:NP275566.RAXOhlowmHbLQo0i0cAxY1xORtBHPcXzH4N81P7CyazOA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:35+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" .
}