@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP541992.RA0mtIGi0wmDSALQGC7M7TwathKFKZKa5J2zaGJXMO75A> .
@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:NP541992.RA0mtIGi0wmDSALQGC7M7TwathKFKZKa5J2zaGJXMO75A130_head {
  this: np:hasAssertion dgn-np:NP541992.RA0mtIGi0wmDSALQGC7M7TwathKFKZKa5J2zaGJXMO75A130_assertion;
    np:hasProvenance dgn-np:NP541992.RA0mtIGi0wmDSALQGC7M7TwathKFKZKa5J2zaGJXMO75A130_provenance;
    np:hasPublicationInfo dgn-np:NP541992.RA0mtIGi0wmDSALQGC7M7TwathKFKZKa5J2zaGJXMO75A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP541992.RA0mtIGi0wmDSALQGC7M7TwathKFKZKa5J2zaGJXMO75A130_assertion a np:Assertion .
  
  dgn-np:NP541992.RA0mtIGi0wmDSALQGC7M7TwathKFKZKa5J2zaGJXMO75A130_provenance a np:Provenance .
  
  dgn-np:NP541992.RA0mtIGi0wmDSALQGC7M7TwathKFKZKa5J2zaGJXMO75A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP541992.RA0mtIGi0wmDSALQGC7M7TwathKFKZKa5J2zaGJXMO75A130_assertion {
  miriam-gene:2944 a ncit:C16612 .
  
  lld:C0029925 a ncit:C7057 .
  
  dgn-gda:DGNb8b91e05e41917a1a687dc09fd9c1671 sio:SIO_000628 miriam-gene:2944, lld:C0029925;
    a sio:SIO_001121 .
}

dgn-np:NP541992.RA0mtIGi0wmDSALQGC7M7TwathKFKZKa5J2zaGJXMO75A130_provenance {
  dgn-np:NP541992.RA0mtIGi0wmDSALQGC7M7TwathKFKZKa5J2zaGJXMO75A130_assertion dcterms:description
      "[To assess the role of GST gene variants in ovarian cancer development, we screened 285 epithelial ovarian cancer cases and 299 unaffected controls for the GSTT1 deletion (null) variant, the GSTM1 deletion (null) variant and the GSTP1 codon 104 A-->G Ile-->Val amino acid substitution variant.]. 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:11159743;
    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:NP541992.RA0mtIGi0wmDSALQGC7M7TwathKFKZKa5J2zaGJXMO75A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:27+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" .
}