@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP62798.RAtB3U0rDFZOPJl1qQM3Jpehr22q5-uBTuafGjBY2JfJE> .
@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:NP62798.RAtB3U0rDFZOPJl1qQM3Jpehr22q5-uBTuafGjBY2JfJE130_head {
  this: np:hasAssertion dgn-np:NP62798.RAtB3U0rDFZOPJl1qQM3Jpehr22q5-uBTuafGjBY2JfJE130_assertion;
    np:hasProvenance dgn-np:NP62798.RAtB3U0rDFZOPJl1qQM3Jpehr22q5-uBTuafGjBY2JfJE130_provenance;
    np:hasPublicationInfo dgn-np:NP62798.RAtB3U0rDFZOPJl1qQM3Jpehr22q5-uBTuafGjBY2JfJE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP62798.RAtB3U0rDFZOPJl1qQM3Jpehr22q5-uBTuafGjBY2JfJE130_assertion a np:Assertion .
  
  dgn-np:NP62798.RAtB3U0rDFZOPJl1qQM3Jpehr22q5-uBTuafGjBY2JfJE130_provenance a np:Provenance .
  
  dgn-np:NP62798.RAtB3U0rDFZOPJl1qQM3Jpehr22q5-uBTuafGjBY2JfJE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP62798.RAtB3U0rDFZOPJl1qQM3Jpehr22q5-uBTuafGjBY2JfJE130_assertion {
  miriam-gene:3265 a ncit:C16612 .
  
  lld:C0242379 a ncit:C7057 .
  
  dgn-gda:DGN2406e4fb98f3984e37045f52d8f9e402 sio:SIO_000628 miriam-gene:3265, lld:C0242379;
    a sio:SIO_001122 .
}

dgn-np:NP62798.RAtB3U0rDFZOPJl1qQM3Jpehr22q5-uBTuafGjBY2JfJE130_provenance {
  dgn-np:NP62798.RAtB3U0rDFZOPJl1qQM3Jpehr22q5-uBTuafGjBY2JfJE130_assertion dcterms:description
      "[This study suggests that the presence of two rare HRAS1 alleles confers an increased lung cancer risk in Native Hawaiians and Japanese but possibly not in Caucasians. The amino acid replacement of arginine by proline at codon 72 of TP53 appears not to be important in determining lung cancer risk in this population.]. 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:11097227;
    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:NP62798.RAtB3U0rDFZOPJl1qQM3Jpehr22q5-uBTuafGjBY2JfJE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:29+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" .
}