@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP178591.RA5IMEcSPVIEQ7pwjJG5VPoz_Rem11hE4hNcSBjcIvq6Y> .
@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:NP178591.RA5IMEcSPVIEQ7pwjJG5VPoz_Rem11hE4hNcSBjcIvq6Y130_head {
  this: np:hasAssertion dgn-np:NP178591.RA5IMEcSPVIEQ7pwjJG5VPoz_Rem11hE4hNcSBjcIvq6Y130_assertion ;
    np:hasProvenance dgn-np:NP178591.RA5IMEcSPVIEQ7pwjJG5VPoz_Rem11hE4hNcSBjcIvq6Y130_provenance ;
    np:hasPublicationInfo dgn-np:NP178591.RA5IMEcSPVIEQ7pwjJG5VPoz_Rem11hE4hNcSBjcIvq6Y130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP178591.RA5IMEcSPVIEQ7pwjJG5VPoz_Rem11hE4hNcSBjcIvq6Y130_assertion a np:Assertion .
  dgn-np:NP178591.RA5IMEcSPVIEQ7pwjJG5VPoz_Rem11hE4hNcSBjcIvq6Y130_provenance a np:Provenance .
  dgn-np:NP178591.RA5IMEcSPVIEQ7pwjJG5VPoz_Rem11hE4hNcSBjcIvq6Y130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP178591.RA5IMEcSPVIEQ7pwjJG5VPoz_Rem11hE4hNcSBjcIvq6Y130_assertion {
  miriam-gene:9083 a ncit:C16612 .
  lld:C0021364 a ncit:C7057 .
  dgn-gda:DGN93ded13503e01ece129218534106ffd4 sio:SIO_000628 miriam-gene:9083 , lld:C0021364 ;
    a sio:SIO_001121 .
}
dgn-np:NP178591.RA5IMEcSPVIEQ7pwjJG5VPoz_Rem11hE4hNcSBjcIvq6Y130_provenance {
  dgn-np:NP178591.RA5IMEcSPVIEQ7pwjJG5VPoz_Rem11hE4hNcSBjcIvq6Y130_assertion dcterms:description "[Partial AZF deletions including single AZF Y genes can cause the same testicular pathology as the corresponding complete deletion (e.g., DDX3Y gene deletions in AZFa), or might not be associated with male infertility at all (e.g., some BPY2, CDY1, DAZ gene deletions in AZFc).]. 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:22992914 ;
    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:NP178591.RA5IMEcSPVIEQ7pwjJG5VPoz_Rem11hE4hNcSBjcIvq6Y130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:36+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" .
}