@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP558611.RAmlQdp7S_j5XAE4jXRnIJwWk3edFqBQWgY9E7l22kF8c> .
@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:NP558611.RAmlQdp7S_j5XAE4jXRnIJwWk3edFqBQWgY9E7l22kF8c130_head {
  this: np:hasAssertion dgn-np:NP558611.RAmlQdp7S_j5XAE4jXRnIJwWk3edFqBQWgY9E7l22kF8c130_assertion ;
    np:hasProvenance dgn-np:NP558611.RAmlQdp7S_j5XAE4jXRnIJwWk3edFqBQWgY9E7l22kF8c130_provenance ;
    np:hasPublicationInfo dgn-np:NP558611.RAmlQdp7S_j5XAE4jXRnIJwWk3edFqBQWgY9E7l22kF8c130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP558611.RAmlQdp7S_j5XAE4jXRnIJwWk3edFqBQWgY9E7l22kF8c130_provenance a np:Provenance .
  dgn-np:NP558611.RAmlQdp7S_j5XAE4jXRnIJwWk3edFqBQWgY9E7l22kF8c130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP558611.RAmlQdp7S_j5XAE4jXRnIJwWk3edFqBQWgY9E7l22kF8c130_assertion {
  miriam-gene:7518 a ncit:C16612 .
  lld:C0021364 a ncit:C7057 .
  dgn-gda:DGN38c96149860eb3e190857186ad1d0ad4 sio:SIO_000628 miriam-gene:7518 , lld:C0021364 ;
    a sio:SIO_001121 .
}
dgn-np:NP558611.RAmlQdp7S_j5XAE4jXRnIJwWk3edFqBQWgY9E7l22kF8c130_provenance {
  dgn-np:NP558611.RAmlQdp7S_j5XAE4jXRnIJwWk3edFqBQWgY9E7l22kF8c130_assertion dcterms:description "[To test the hypothesis that polymorphisms in DSBs genes are associated with susceptibility to male infertility, we examined 11 single nucleotide polymorphisms in eight key DSBs genes (XRCC3, XRCC2, BRCA2, RAG1, XRCC5, LIG4, XRCC4 and ATM) in 580 infertility cases and 580 controls from a Chinese population-based case-control study (NJMU Infertility Study).]. 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:23630330 ;
    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:NP558611.RAmlQdp7S_j5XAE4jXRnIJwWk3edFqBQWgY9E7l22kF8c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:37+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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