@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP490197.RAw6cFlir9Xy4eqBrDXtDGUNeyzn8TAASJWYcsoeOgYJk> .
@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:NP490197.RAw6cFlir9Xy4eqBrDXtDGUNeyzn8TAASJWYcsoeOgYJk130_head {
  this: np:hasAssertion dgn-np:NP490197.RAw6cFlir9Xy4eqBrDXtDGUNeyzn8TAASJWYcsoeOgYJk130_assertion;
    np:hasProvenance dgn-np:NP490197.RAw6cFlir9Xy4eqBrDXtDGUNeyzn8TAASJWYcsoeOgYJk130_provenance;
    np:hasPublicationInfo dgn-np:NP490197.RAw6cFlir9Xy4eqBrDXtDGUNeyzn8TAASJWYcsoeOgYJk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP490197.RAw6cFlir9Xy4eqBrDXtDGUNeyzn8TAASJWYcsoeOgYJk130_assertion a np:Assertion .
  
  dgn-np:NP490197.RAw6cFlir9Xy4eqBrDXtDGUNeyzn8TAASJWYcsoeOgYJk130_provenance a np:Provenance .
  
  dgn-np:NP490197.RAw6cFlir9Xy4eqBrDXtDGUNeyzn8TAASJWYcsoeOgYJk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP490197.RAw6cFlir9Xy4eqBrDXtDGUNeyzn8TAASJWYcsoeOgYJk130_assertion {
  miriam-gene:10544 a ncit:C16612 .
  
  lld:C0684249 a ncit:C7057 .
  
  dgn-gda:DGNaf790fb8f7d7a7497f4568770f1db42a sio:SIO_000628 miriam-gene:10544, lld:C0684249;
    a sio:SIO_001121 .
}

dgn-np:NP490197.RAw6cFlir9Xy4eqBrDXtDGUNeyzn8TAASJWYcsoeOgYJk130_provenance {
  dgn-np:NP490197.RAw6cFlir9Xy4eqBrDXtDGUNeyzn8TAASJWYcsoeOgYJk130_assertion dcterms:description
      "[Using enriched PCR (EPCR), which enables the detection of one mutant allele in the presence of 10,000 normal alleles, we have determined the frequency of mutant ras alleles in the sputum samples of patients with or without lung cancer.]. 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:9027615;
    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:NP490197.RAw6cFlir9Xy4eqBrDXtDGUNeyzn8TAASJWYcsoeOgYJk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:53+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" .
}