@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP423428.RAgx2YB5MDBq5CYXnjzsIbdpPzJ0sm3UN5fqF0hLPr1xY> .
@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:NP423428.RAgx2YB5MDBq5CYXnjzsIbdpPzJ0sm3UN5fqF0hLPr1xY130_head {
  this: np:hasAssertion dgn-np:NP423428.RAgx2YB5MDBq5CYXnjzsIbdpPzJ0sm3UN5fqF0hLPr1xY130_assertion;
    np:hasProvenance dgn-np:NP423428.RAgx2YB5MDBq5CYXnjzsIbdpPzJ0sm3UN5fqF0hLPr1xY130_provenance;
    np:hasPublicationInfo dgn-np:NP423428.RAgx2YB5MDBq5CYXnjzsIbdpPzJ0sm3UN5fqF0hLPr1xY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP423428.RAgx2YB5MDBq5CYXnjzsIbdpPzJ0sm3UN5fqF0hLPr1xY130_assertion a np:Assertion .
  
  dgn-np:NP423428.RAgx2YB5MDBq5CYXnjzsIbdpPzJ0sm3UN5fqF0hLPr1xY130_provenance a np:Provenance .
  
  dgn-np:NP423428.RAgx2YB5MDBq5CYXnjzsIbdpPzJ0sm3UN5fqF0hLPr1xY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP423428.RAgx2YB5MDBq5CYXnjzsIbdpPzJ0sm3UN5fqF0hLPr1xY130_assertion {
  miriam-gene:27030 a ncit:C16612 .
  
  lld:C0004509 a ncit:C7057 .
  
  dgn-gda:DGN10670b9f1335ab146436c74d3f957a34 sio:SIO_000628 miriam-gene:27030, lld:C0004509;
    a sio:SIO_001121 .
}

dgn-np:NP423428.RAgx2YB5MDBq5CYXnjzsIbdpPzJ0sm3UN5fqF0hLPr1xY130_provenance {
  dgn-np:NP423428.RAgx2YB5MDBq5CYXnjzsIbdpPzJ0sm3UN5fqF0hLPr1xY130_assertion dcterms:description
      "[There is an association of polymorphism C85T in MSH5 or C2531T in MLH3 with male infertility, specifically azoospermia or severe oligozoospermia, and interaction between these MSH5 and MLH3 polymorphisms increased the risk of developing 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:19808033;
    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:NP423428.RAgx2YB5MDBq5CYXnjzsIbdpPzJ0sm3UN5fqF0hLPr1xY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:11+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>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}