@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP53043.RALEVHKkGVFYoJ3DFbckW4bwDj-wVfAO2HonYCF21bP1w> .
@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:NP53043.RALEVHKkGVFYoJ3DFbckW4bwDj-wVfAO2HonYCF21bP1w130_head {
  this: np:hasAssertion dgn-np:NP53043.RALEVHKkGVFYoJ3DFbckW4bwDj-wVfAO2HonYCF21bP1w130_assertion;
    np:hasProvenance dgn-np:NP53043.RALEVHKkGVFYoJ3DFbckW4bwDj-wVfAO2HonYCF21bP1w130_provenance;
    np:hasPublicationInfo dgn-np:NP53043.RALEVHKkGVFYoJ3DFbckW4bwDj-wVfAO2HonYCF21bP1w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP53043.RALEVHKkGVFYoJ3DFbckW4bwDj-wVfAO2HonYCF21bP1w130_assertion a np:Assertion .
  
  dgn-np:NP53043.RALEVHKkGVFYoJ3DFbckW4bwDj-wVfAO2HonYCF21bP1w130_provenance a np:Provenance .
  
  dgn-np:NP53043.RALEVHKkGVFYoJ3DFbckW4bwDj-wVfAO2HonYCF21bP1w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP53043.RALEVHKkGVFYoJ3DFbckW4bwDj-wVfAO2HonYCF21bP1w130_assertion {
  miriam-gene:5428 a ncit:C16612 .
  
  lld:C0021364 a ncit:C7057 .
  
  dgn-gda:DGNcde695716a68e2dcc713a783758a9107 sio:SIO_000628 miriam-gene:5428, lld:C0021364;
    a sio:SIO_001122 .
}

dgn-np:NP53043.RALEVHKkGVFYoJ3DFbckW4bwDj-wVfAO2HonYCF21bP1w130_provenance {
  dgn-np:NP53043.RALEVHKkGVFYoJ3DFbckW4bwDj-wVfAO2HonYCF21bP1w130_assertion dcterms:description
      "[Our findings have shown for the first time that there exits an ethnic difference between Chinese and European males in the number of CAG repeats of Polg gene, and that 10/not 10 CAG genotype may affect sperm motility.]. 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:16970152;
    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:NP53043.RALEVHKkGVFYoJ3DFbckW4bwDj-wVfAO2HonYCF21bP1w130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:24+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" .
}