@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP713729.RAgCyTltbQ6BZXhg9Ie885pWEi7Hm3m6rw6O1_2E-GVJc> .
@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:NP713729.RAgCyTltbQ6BZXhg9Ie885pWEi7Hm3m6rw6O1_2E-GVJc130_head {
  this: np:hasAssertion dgn-np:NP713729.RAgCyTltbQ6BZXhg9Ie885pWEi7Hm3m6rw6O1_2E-GVJc130_assertion ;
    np:hasProvenance dgn-np:NP713729.RAgCyTltbQ6BZXhg9Ie885pWEi7Hm3m6rw6O1_2E-GVJc130_provenance ;
    np:hasPublicationInfo dgn-np:NP713729.RAgCyTltbQ6BZXhg9Ie885pWEi7Hm3m6rw6O1_2E-GVJc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP713729.RAgCyTltbQ6BZXhg9Ie885pWEi7Hm3m6rw6O1_2E-GVJc130_assertion a np:Assertion .
  dgn-np:NP713729.RAgCyTltbQ6BZXhg9Ie885pWEi7Hm3m6rw6O1_2E-GVJc130_provenance a np:Provenance .
  dgn-np:NP713729.RAgCyTltbQ6BZXhg9Ie885pWEi7Hm3m6rw6O1_2E-GVJc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP713729.RAgCyTltbQ6BZXhg9Ie885pWEi7Hm3m6rw6O1_2E-GVJc130_assertion {
  miriam-gene:412 a ncit:C16612 .
  lld:C0021359 a ncit:C7057 .
  dgn-gda:DGNd9f5637636ff2dc1237508039589e083 sio:SIO_000628 miriam-gene:412 , lld:C0021359 ;
    a sio:SIO_001121 .
}
dgn-np:NP713729.RAgCyTltbQ6BZXhg9Ie885pWEi7Hm3m6rw6O1_2E-GVJc130_provenance {
  dgn-np:NP713729.RAgCyTltbQ6BZXhg9Ie885pWEi7Hm3m6rw6O1_2E-GVJc130_assertion dcterms:description "[To determine the prevalence of Y-chromosome microdeletions among infertile men and to correlate the clinical presentation of the men with specific deletions, microdeletion analysis in 53 infertile men (30 nonobstructive azoospermic, 23 severely oligozoospermic patients), and 100 age-matched, fathered normospermic men who had fathered children was performed by the multiplex PCR with 18 different Y-chromosome-specific STS primer sets, spanning the AZFa, AZFb, AZFd, and AZFc regions.]. 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:16084901 ;
    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:NP713729.RAgCyTltbQ6BZXhg9Ie885pWEi7Hm3m6rw6O1_2E-GVJc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:13+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> ;
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    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}