@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP320345.RAhzs-wn4VmvG_g-i8oKaVwIO5ZVLQd1opnFjpqf4WNXY> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP320345.RAhzs-wn4VmvG_g-i8oKaVwIO5ZVLQd1opnFjpqf4WNXY130_head {
  this: np:hasAssertion dgn-np:NP320345.RAhzs-wn4VmvG_g-i8oKaVwIO5ZVLQd1opnFjpqf4WNXY130_assertion ;
    np:hasProvenance dgn-np:NP320345.RAhzs-wn4VmvG_g-i8oKaVwIO5ZVLQd1opnFjpqf4WNXY130_provenance ;
    np:hasPublicationInfo dgn-np:NP320345.RAhzs-wn4VmvG_g-i8oKaVwIO5ZVLQd1opnFjpqf4WNXY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP320345.RAhzs-wn4VmvG_g-i8oKaVwIO5ZVLQd1opnFjpqf4WNXY130_assertion a np:Assertion .
  dgn-np:NP320345.RAhzs-wn4VmvG_g-i8oKaVwIO5ZVLQd1opnFjpqf4WNXY130_provenance a np:Provenance .
  dgn-np:NP320345.RAhzs-wn4VmvG_g-i8oKaVwIO5ZVLQd1opnFjpqf4WNXY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP320345.RAhzs-wn4VmvG_g-i8oKaVwIO5ZVLQd1opnFjpqf4WNXY130_assertion {
  miriam-gene:100653377 a ncit:C16612 .
  lld:C0028960 a ncit:C7057 .
  dgn-gda:DGNe5decaa31062bdf4c2c22fee63b76d7b sio:SIO_000628 miriam-gene:100653377 , lld:C0028960 ;
    a sio:SIO_001121 .
}
dgn-np:NP320345.RAhzs-wn4VmvG_g-i8oKaVwIO5ZVLQd1opnFjpqf4WNXY130_provenance {
  dgn-np:NP320345.RAhzs-wn4VmvG_g-i8oKaVwIO5ZVLQd1opnFjpqf4WNXY130_assertion dcterms:description "[The data indicate that: 1) the composition of the study population is the major factor in determining deletion frequency; 2) Y chromosome microdeletions are specifically associated with severe spermatogenic failure; therefore, the protocol described here is reliable for the routine clinical workup of severe male factor infertility; and 3) the frequency of Yq microdeletions in the Danish population is similar to that from other countries and argues against the involvement of microdeletions in the relatively low sperm count of the Danish population.]. 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:11397865 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP320345.RAhzs-wn4VmvG_g-i8oKaVwIO5ZVLQd1opnFjpqf4WNXY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:10+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}