@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP892950.RA2m5rTCTaTVKyS-0ybZFW1dj5WVq6gsiE1yEjkfTCE_I> .
@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:NP892950.RA2m5rTCTaTVKyS-0ybZFW1dj5WVq6gsiE1yEjkfTCE_I130_head {
  this: np:hasAssertion dgn-np:NP892950.RA2m5rTCTaTVKyS-0ybZFW1dj5WVq6gsiE1yEjkfTCE_I130_assertion;
    np:hasProvenance dgn-np:NP892950.RA2m5rTCTaTVKyS-0ybZFW1dj5WVq6gsiE1yEjkfTCE_I130_provenance;
    np:hasPublicationInfo dgn-np:NP892950.RA2m5rTCTaTVKyS-0ybZFW1dj5WVq6gsiE1yEjkfTCE_I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP892950.RA2m5rTCTaTVKyS-0ybZFW1dj5WVq6gsiE1yEjkfTCE_I130_assertion a np:Assertion .
  
  dgn-np:NP892950.RA2m5rTCTaTVKyS-0ybZFW1dj5WVq6gsiE1yEjkfTCE_I130_provenance a np:Provenance .
  
  dgn-np:NP892950.RA2m5rTCTaTVKyS-0ybZFW1dj5WVq6gsiE1yEjkfTCE_I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP892950.RA2m5rTCTaTVKyS-0ybZFW1dj5WVq6gsiE1yEjkfTCE_I130_assertion {
  miriam-gene:4942 a ncit:C16612 .
  
  lld:C0008626 a ncit:C7057 .
  
  dgn-gda:DGNc5a06390e948635ce2e13e57bc6552a4 sio:SIO_000628 miriam-gene:4942, lld:C0008626;
    a sio:SIO_001121 .
}

dgn-np:NP892950.RA2m5rTCTaTVKyS-0ybZFW1dj5WVq6gsiE1yEjkfTCE_I130_provenance {
  dgn-np:NP892950.RA2m5rTCTaTVKyS-0ybZFW1dj5WVq6gsiE1yEjkfTCE_I130_assertion dcterms:description
      "[Our data suggest that: (i) chromosome abnormalities observed in spermatozoa of the two XYY oligoasthenoteratospermic (OAT) males arise through segregation errors in XY germ cells rather than normal meiosis of XYY germ cells, (ii) mosaic XYY males with normal semen parameters have a lower risk of producing offspring with a sex chromosomal abnormality than OAT males with XYY karyotype.]. 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:12846800;
    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:NP892950.RA2m5rTCTaTVKyS-0ybZFW1dj5WVq6gsiE1yEjkfTCE_I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:09+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" .
}