@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP723397.RAsy_y3o1Q0dQ3ePqOgMoJlwDp89aZ28efR62Ov1AdPCY> .
@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:NP723397.RAsy_y3o1Q0dQ3ePqOgMoJlwDp89aZ28efR62Ov1AdPCY130_head {
  this: np:hasAssertion dgn-np:NP723397.RAsy_y3o1Q0dQ3ePqOgMoJlwDp89aZ28efR62Ov1AdPCY130_assertion;
    np:hasProvenance dgn-np:NP723397.RAsy_y3o1Q0dQ3ePqOgMoJlwDp89aZ28efR62Ov1AdPCY130_provenance;
    np:hasPublicationInfo dgn-np:NP723397.RAsy_y3o1Q0dQ3ePqOgMoJlwDp89aZ28efR62Ov1AdPCY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP723397.RAsy_y3o1Q0dQ3ePqOgMoJlwDp89aZ28efR62Ov1AdPCY130_assertion a np:Assertion .
  
  dgn-np:NP723397.RAsy_y3o1Q0dQ3ePqOgMoJlwDp89aZ28efR62Ov1AdPCY130_provenance a np:Provenance .
  
  dgn-np:NP723397.RAsy_y3o1Q0dQ3ePqOgMoJlwDp89aZ28efR62Ov1AdPCY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP723397.RAsy_y3o1Q0dQ3ePqOgMoJlwDp89aZ28efR62Ov1AdPCY130_assertion {
  miriam-gene:9083 a ncit:C16612 .
  
  lld:C0021359 a ncit:C7057 .
  
  dgn-gda:DGNf1563e9cd18e79241af0fede04da3406 sio:SIO_000628 miriam-gene:9083, lld:C0021359;
    a sio:SIO_001121 .
}

dgn-np:NP723397.RAsy_y3o1Q0dQ3ePqOgMoJlwDp89aZ28efR62Ov1AdPCY130_provenance {
  dgn-np:NP723397.RAsy_y3o1Q0dQ3ePqOgMoJlwDp89aZ28efR62Ov1AdPCY130_assertion dcterms:description
      "[PCR, Southern blot, and FISH analysis on infertile patients with Yq microdeletions demonstrated the absence of VCY2 in all cases where deletions involved the DAZ gene, raising the question about the role of the VCY2 gene loss in the phenotype reported for DAZ-deleted patients.]. 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:11401428;
    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:NP723397.RAsy_y3o1Q0dQ3ePqOgMoJlwDp89aZ28efR62Ov1AdPCY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:19+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" .
}