@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP266159.RAvjduPjCof4me2Fk_uA41Yt0IWuIWVAfhg7sDVAOIWfg> .
@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:NP266159.RAvjduPjCof4me2Fk_uA41Yt0IWuIWVAfhg7sDVAOIWfg130_head {
  this: np:hasAssertion dgn-np:NP266159.RAvjduPjCof4me2Fk_uA41Yt0IWuIWVAfhg7sDVAOIWfg130_assertion;
    np:hasProvenance dgn-np:NP266159.RAvjduPjCof4me2Fk_uA41Yt0IWuIWVAfhg7sDVAOIWfg130_provenance;
    np:hasPublicationInfo dgn-np:NP266159.RAvjduPjCof4me2Fk_uA41Yt0IWuIWVAfhg7sDVAOIWfg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP266159.RAvjduPjCof4me2Fk_uA41Yt0IWuIWVAfhg7sDVAOIWfg130_assertion a np:Assertion .
  
  dgn-np:NP266159.RAvjduPjCof4me2Fk_uA41Yt0IWuIWVAfhg7sDVAOIWfg130_provenance a np:Provenance .
  
  dgn-np:NP266159.RAvjduPjCof4me2Fk_uA41Yt0IWuIWVAfhg7sDVAOIWfg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP266159.RAvjduPjCof4me2Fk_uA41Yt0IWuIWVAfhg7sDVAOIWfg130_assertion {
  miriam-gene:8852 a ncit:C16612 .
  
  lld:C0021359 a ncit:C7057 .
  
  dgn-gda:DGNf680940f0a500211a549abb9c6a838e8 sio:SIO_000628 miriam-gene:8852, lld:C0021359;
    a sio:SIO_001121 .
}

dgn-np:NP266159.RAvjduPjCof4me2Fk_uA41Yt0IWuIWVAfhg7sDVAOIWfg130_provenance {
  dgn-np:NP266159.RAvjduPjCof4me2Fk_uA41Yt0IWuIWVAfhg7sDVAOIWfg130_assertion dcterms:description
      "[We report the case of an infertile man with normal sperm count and total sperm immotility in which dysplasia of the fibrous sheath, Akap3, Akap4 gene deletions, meiotic segregation of chromosomes 18, X and Y and Y microdeletions were investigated.]. 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:15980003;
    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:NP266159.RAvjduPjCof4me2Fk_uA41Yt0IWuIWVAfhg7sDVAOIWfg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:28+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" .
}