@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP50747.RAq0ERH2IUcDyTFdEm99vRtGfhP4VdkrBksaGq1CKITo4> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP50747.RAq0ERH2IUcDyTFdEm99vRtGfhP4VdkrBksaGq1CKITo4130_head {
  this: np:hasAssertion dgn-np:NP50747.RAq0ERH2IUcDyTFdEm99vRtGfhP4VdkrBksaGq1CKITo4130_assertion;
    np:hasProvenance dgn-np:NP50747.RAq0ERH2IUcDyTFdEm99vRtGfhP4VdkrBksaGq1CKITo4130_provenance;
    np:hasPublicationInfo dgn-np:NP50747.RAq0ERH2IUcDyTFdEm99vRtGfhP4VdkrBksaGq1CKITo4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP50747.RAq0ERH2IUcDyTFdEm99vRtGfhP4VdkrBksaGq1CKITo4130_assertion a np:Assertion .
  
  dgn-np:NP50747.RAq0ERH2IUcDyTFdEm99vRtGfhP4VdkrBksaGq1CKITo4130_provenance a np:Provenance .
  
  dgn-np:NP50747.RAq0ERH2IUcDyTFdEm99vRtGfhP4VdkrBksaGq1CKITo4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP50747.RAq0ERH2IUcDyTFdEm99vRtGfhP4VdkrBksaGq1CKITo4130_assertion {
  miriam-gene:9446 a ncit:C16612 .
  
  lld:C0020179 a ncit:C7057 .
  
  dgn-gda:DGN12cefb73dce6f3c209900145c366832e sio:SIO_000628 miriam-gene:9446, lld:C0020179;
    a sio:SIO_001122 .
}

dgn-np:NP50747.RAq0ERH2IUcDyTFdEm99vRtGfhP4VdkrBksaGq1CKITo4130_provenance {
  dgn-np:NP50747.RAq0ERH2IUcDyTFdEm99vRtGfhP4VdkrBksaGq1CKITo4130_assertion dcterms:description
      "[After genotyping GSTO1 and GSTO2 polymorphisms, firstly there was no statistically significant difference in AO for HD patients, as well as secondly for HD patients vs. controls concerning, both, genotype and allele frequencies, respectively.]. 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:15040808;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP50747.RAq0ERH2IUcDyTFdEm99vRtGfhP4VdkrBksaGq1CKITo4130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:08+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}