@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP183220.RAQ5jdF2Xj9VUYVtjO_D-qtkGiyqZLeZ2GxP4TBrKviQU> .
@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:NP183220.RAQ5jdF2Xj9VUYVtjO_D-qtkGiyqZLeZ2GxP4TBrKviQU130_head {
  this: np:hasAssertion dgn-np:NP183220.RAQ5jdF2Xj9VUYVtjO_D-qtkGiyqZLeZ2GxP4TBrKviQU130_assertion;
    np:hasProvenance dgn-np:NP183220.RAQ5jdF2Xj9VUYVtjO_D-qtkGiyqZLeZ2GxP4TBrKviQU130_provenance;
    np:hasPublicationInfo dgn-np:NP183220.RAQ5jdF2Xj9VUYVtjO_D-qtkGiyqZLeZ2GxP4TBrKviQU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP183220.RAQ5jdF2Xj9VUYVtjO_D-qtkGiyqZLeZ2GxP4TBrKviQU130_assertion a np:Assertion .
  
  dgn-np:NP183220.RAQ5jdF2Xj9VUYVtjO_D-qtkGiyqZLeZ2GxP4TBrKviQU130_provenance a np:Provenance .
  
  dgn-np:NP183220.RAQ5jdF2Xj9VUYVtjO_D-qtkGiyqZLeZ2GxP4TBrKviQU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP183220.RAQ5jdF2Xj9VUYVtjO_D-qtkGiyqZLeZ2GxP4TBrKviQU130_assertion {
  miriam-gene:7063 a ncit:C16612 .
  
  lld:C0007097 a ncit:C7057 .
  
  dgn-gda:DGN05b5cce4734cae58986a6545828cbd61 sio:SIO_000628 miriam-gene:7063, lld:C0007097;
    a sio:SIO_001121 .
}

dgn-np:NP183220.RAQ5jdF2Xj9VUYVtjO_D-qtkGiyqZLeZ2GxP4TBrKviQU130_provenance {
  dgn-np:NP183220.RAQ5jdF2Xj9VUYVtjO_D-qtkGiyqZLeZ2GxP4TBrKviQU130_assertion dcterms:description
      "[Occasional point mutations in ras oncogenes were detected in adenosquamous carcinomas (one of five cases) and large cell carcinoma (one of 24 cases), but no ras activations were found in small cell carcinomas (six cases), squamous carcinomas (48 cases), carcinoid carcinomas (15 cases), or thymoma (one case).]. 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:1562997;
    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:NP183220.RAQ5jdF2Xj9VUYVtjO_D-qtkGiyqZLeZ2GxP4TBrKviQU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:39+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" .
}