@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP523604.RA3m2yvgWnoc3dsqIXUWjYo9c81ci05rdogVXKbz575x4> .
@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:NP523604.RA3m2yvgWnoc3dsqIXUWjYo9c81ci05rdogVXKbz575x4130_head {
  this: np:hasAssertion dgn-np:NP523604.RA3m2yvgWnoc3dsqIXUWjYo9c81ci05rdogVXKbz575x4130_assertion;
    np:hasProvenance dgn-np:NP523604.RA3m2yvgWnoc3dsqIXUWjYo9c81ci05rdogVXKbz575x4130_provenance;
    np:hasPublicationInfo dgn-np:NP523604.RA3m2yvgWnoc3dsqIXUWjYo9c81ci05rdogVXKbz575x4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP523604.RA3m2yvgWnoc3dsqIXUWjYo9c81ci05rdogVXKbz575x4130_assertion a np:Assertion .
  
  dgn-np:NP523604.RA3m2yvgWnoc3dsqIXUWjYo9c81ci05rdogVXKbz575x4130_provenance a np:Provenance .
  
  dgn-np:NP523604.RA3m2yvgWnoc3dsqIXUWjYo9c81ci05rdogVXKbz575x4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP523604.RA3m2yvgWnoc3dsqIXUWjYo9c81ci05rdogVXKbz575x4130_assertion {
  miriam-gene:2952 a ncit:C16612 .
  
  lld:C0032927 a ncit:C7057 .
  
  dgn-gda:DGNb6fe7ed4bef804c74514b2f6bc6ab8b8 sio:SIO_000628 miriam-gene:2952, lld:C0032927;
    a sio:SIO_001121 .
}

dgn-np:NP523604.RA3m2yvgWnoc3dsqIXUWjYo9c81ci05rdogVXKbz575x4130_provenance {
  dgn-np:NP523604.RA3m2yvgWnoc3dsqIXUWjYo9c81ci05rdogVXKbz575x4130_assertion dcterms:description
      "[The PCR study revealed that there is no significant difference in the allelic variants in GSTM1 between OSF and normal, while GSTT1 null gene showed significantly higher frequencies in this precancerous condition.]. 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:18573513;
    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:NP523604.RA3m2yvgWnoc3dsqIXUWjYo9c81ci05rdogVXKbz575x4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:14+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" .
}