@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP892298.RAUsQLQBan_t4g-Bv6C1S48cAYZepcABK5-X4kKCMr8nk> .
@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:NP892298.RAUsQLQBan_t4g-Bv6C1S48cAYZepcABK5-X4kKCMr8nk130_head {
  this: np:hasAssertion dgn-np:NP892298.RAUsQLQBan_t4g-Bv6C1S48cAYZepcABK5-X4kKCMr8nk130_assertion ;
    np:hasProvenance dgn-np:NP892298.RAUsQLQBan_t4g-Bv6C1S48cAYZepcABK5-X4kKCMr8nk130_provenance ;
    np:hasPublicationInfo dgn-np:NP892298.RAUsQLQBan_t4g-Bv6C1S48cAYZepcABK5-X4kKCMr8nk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP892298.RAUsQLQBan_t4g-Bv6C1S48cAYZepcABK5-X4kKCMr8nk130_assertion a np:Assertion .
  dgn-np:NP892298.RAUsQLQBan_t4g-Bv6C1S48cAYZepcABK5-X4kKCMr8nk130_provenance a np:Provenance .
  dgn-np:NP892298.RAUsQLQBan_t4g-Bv6C1S48cAYZepcABK5-X4kKCMr8nk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP892298.RAUsQLQBan_t4g-Bv6C1S48cAYZepcABK5-X4kKCMr8nk130_assertion {
  miriam-gene:66037 a ncit:C16612 .
  lld:C0018889 a ncit:C7057 .
  dgn-gda:DGN0d02200cdfe735b7a468d4adde56fbcb sio:SIO_000628 miriam-gene:66037 , lld:C0018889 ;
    a sio:SIO_001121 .
}
dgn-np:NP892298.RAUsQLQBan_t4g-Bv6C1S48cAYZepcABK5-X4kKCMr8nk130_provenance {
  dgn-np:NP892298.RAUsQLQBan_t4g-Bv6C1S48cAYZepcABK5-X4kKCMr8nk130_assertion dcterms:description "[As in flies and worms, disruption of the BOULE homologues leads to meiotic defects during the first meiotic division, we screened the coding region of the BOULE gene from 40 infertile men with non-obstructive azoospermia or severe oligoasthenoteratozoospermia by denaturing high-pressure liquid chromatography and direct sequencing in order to make progress in elucidating the aetiology of male infertility.]. 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:15379971 ;
    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:NP892298.RAUsQLQBan_t4g-Bv6C1S48cAYZepcABK5-X4kKCMr8nk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:08+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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}