@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP75409.RANjfP25QzhyGYCjMxiFVedDnJQTG5tbhPsVF5ukRcqpw> .
@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:NP75409.RANjfP25QzhyGYCjMxiFVedDnJQTG5tbhPsVF5ukRcqpw130_head {
  this: np:hasAssertion dgn-np:NP75409.RANjfP25QzhyGYCjMxiFVedDnJQTG5tbhPsVF5ukRcqpw130_assertion;
    np:hasProvenance dgn-np:NP75409.RANjfP25QzhyGYCjMxiFVedDnJQTG5tbhPsVF5ukRcqpw130_provenance;
    np:hasPublicationInfo dgn-np:NP75409.RANjfP25QzhyGYCjMxiFVedDnJQTG5tbhPsVF5ukRcqpw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP75409.RANjfP25QzhyGYCjMxiFVedDnJQTG5tbhPsVF5ukRcqpw130_assertion a np:Assertion .
  
  dgn-np:NP75409.RANjfP25QzhyGYCjMxiFVedDnJQTG5tbhPsVF5ukRcqpw130_provenance a np:Provenance .
  
  dgn-np:NP75409.RANjfP25QzhyGYCjMxiFVedDnJQTG5tbhPsVF5ukRcqpw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP75409.RANjfP25QzhyGYCjMxiFVedDnJQTG5tbhPsVF5ukRcqpw130_assertion {
  miriam-gene:2068 a ncit:C16612 .
  
  lld:C1961102 a ncit:C7057 .
  
  dgn-gda:DGN6a05bd6bb3870e8e9588b617cb085237 sio:SIO_000628 miriam-gene:2068, lld:C1961102;
    a sio:SIO_001122 .
}

dgn-np:NP75409.RANjfP25QzhyGYCjMxiFVedDnJQTG5tbhPsVF5ukRcqpw130_provenance {
  dgn-np:NP75409.RANjfP25QzhyGYCjMxiFVedDnJQTG5tbhPsVF5ukRcqpw130_assertion dcterms:description
      "[We used polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP), to analyze XPD Asp312Asn, XPD Lys751Gln, XRCC1 Arg194Trp, and XRCC1 Arg399Gln polymorphisms in 70 patients with childhood ALL and in 75 disease-free controls, who were of a similar age.]. 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:19101034;
    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:NP75409.RANjfP25QzhyGYCjMxiFVedDnJQTG5tbhPsVF5ukRcqpw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:36+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" .
}