@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP78201.RApD4CayZAOjQBLy6Ca26omOZ_97raiA2FoOVSDJnjWeM> .
@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 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:NP78201.RApD4CayZAOjQBLy6Ca26omOZ_97raiA2FoOVSDJnjWeM130_head {
  this: np:hasAssertion dgn-np:NP78201.RApD4CayZAOjQBLy6Ca26omOZ_97raiA2FoOVSDJnjWeM130_assertion;
    np:hasProvenance dgn-np:NP78201.RApD4CayZAOjQBLy6Ca26omOZ_97raiA2FoOVSDJnjWeM130_provenance;
    np:hasPublicationInfo dgn-np:NP78201.RApD4CayZAOjQBLy6Ca26omOZ_97raiA2FoOVSDJnjWeM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP78201.RApD4CayZAOjQBLy6Ca26omOZ_97raiA2FoOVSDJnjWeM130_assertion a np:Assertion .
  
  dgn-np:NP78201.RApD4CayZAOjQBLy6Ca26omOZ_97raiA2FoOVSDJnjWeM130_provenance a np:Provenance .
  
  dgn-np:NP78201.RApD4CayZAOjQBLy6Ca26omOZ_97raiA2FoOVSDJnjWeM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP78201.RApD4CayZAOjQBLy6Ca26omOZ_97raiA2FoOVSDJnjWeM130_assertion {
  miriam-gene:51087 a ncit:C16612 .
  
  lld:C0021364 a ncit:C7057 .
  
  dgn-gda:DGN57d4c38cc9a46b96d06ddcca1057c0fc sio:SIO_000628 miriam-gene:51087, lld:C0021364;
    a sio:SIO_001122 .
}

dgn-np:NP78201.RApD4CayZAOjQBLy6Ca26omOZ_97raiA2FoOVSDJnjWeM130_provenance {
  dgn-np:NP78201.RApD4CayZAOjQBLy6Ca26omOZ_97raiA2FoOVSDJnjWeM130_assertion dc:description
      "[The results of our study suggest that some polymorphisms of the MSY2 gene might be associated with impaired spermatogenesis and that the gene could also be involved in modifying the susceptibility to idiopathic spermatogenic impairment in humans.]. 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:18372033;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP78201.RApD4CayZAOjQBLy6Ca26omOZ_97raiA2FoOVSDJnjWeM130_publicationInfo {
  this: dc:created "2014-10-02T12:32:38+02:00"^^xsd:dateTime;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dc:rightsHolder dgn-void:IBIGroup;
    dc: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" .
}