@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP59451.RA4V91F9XxEqI-C0EHvfVdBG6fNrrq8p8SC-ufaTB96nA> .
@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 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:NP59451.RA4V91F9XxEqI-C0EHvfVdBG6fNrrq8p8SC-ufaTB96nA130_head {
  this: np:hasAssertion dgn-np:NP59451.RA4V91F9XxEqI-C0EHvfVdBG6fNrrq8p8SC-ufaTB96nA130_assertion;
    np:hasProvenance dgn-np:NP59451.RA4V91F9XxEqI-C0EHvfVdBG6fNrrq8p8SC-ufaTB96nA130_provenance;
    np:hasPublicationInfo dgn-np:NP59451.RA4V91F9XxEqI-C0EHvfVdBG6fNrrq8p8SC-ufaTB96nA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP59451.RA4V91F9XxEqI-C0EHvfVdBG6fNrrq8p8SC-ufaTB96nA130_assertion a np:Assertion .
  
  dgn-np:NP59451.RA4V91F9XxEqI-C0EHvfVdBG6fNrrq8p8SC-ufaTB96nA130_provenance a np:Provenance .
  
  dgn-np:NP59451.RA4V91F9XxEqI-C0EHvfVdBG6fNrrq8p8SC-ufaTB96nA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP59451.RA4V91F9XxEqI-C0EHvfVdBG6fNrrq8p8SC-ufaTB96nA130_assertion {
  miriam-gene:7515 a ncit:C16612 .
  
  lld:C0025286 a ncit:C7057 .
  
  dgn-gda:DGNd5cd619190fccc6afab6c24df890ec77 sio:SIO_000628 miriam-gene:7515, lld:C0025286;
    a sio:SIO_001122 .
}

dgn-np:NP59451.RA4V91F9XxEqI-C0EHvfVdBG6fNrrq8p8SC-ufaTB96nA130_provenance {
  dgn-np:NP59451.RA4V91F9XxEqI-C0EHvfVdBG6fNrrq8p8SC-ufaTB96nA130_assertion dct:description
      "[Our findings suggest that Ki-ras and ERCC2 SNPs are possible markers for meningioma formation, whereas cyclin D1 and p16 SNPs may be markers of genes that have an inverse effect on the risk to develop meningioma in irradiated and nonirradiated populations.]. 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:15824172;
    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:NP59451.RA4V91F9XxEqI-C0EHvfVdBG6fNrrq8p8SC-ufaTB96nA130_publicationInfo {
  this: dct:created "2014-10-02T12:32:28+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}