@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP884607.RASEn6DLliuBc-QhpP2VinYnKTUOU7X3zG3PlLsbzRoIg> .
@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:NP884607.RASEn6DLliuBc-QhpP2VinYnKTUOU7X3zG3PlLsbzRoIg130_head {
  this: np:hasAssertion dgn-np:NP884607.RASEn6DLliuBc-QhpP2VinYnKTUOU7X3zG3PlLsbzRoIg130_assertion;
    np:hasProvenance dgn-np:NP884607.RASEn6DLliuBc-QhpP2VinYnKTUOU7X3zG3PlLsbzRoIg130_provenance;
    np:hasPublicationInfo dgn-np:NP884607.RASEn6DLliuBc-QhpP2VinYnKTUOU7X3zG3PlLsbzRoIg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP884607.RASEn6DLliuBc-QhpP2VinYnKTUOU7X3zG3PlLsbzRoIg130_assertion a np:Assertion .
  
  dgn-np:NP884607.RASEn6DLliuBc-QhpP2VinYnKTUOU7X3zG3PlLsbzRoIg130_provenance a np:Provenance .
  
  dgn-np:NP884607.RASEn6DLliuBc-QhpP2VinYnKTUOU7X3zG3PlLsbzRoIg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP884607.RASEn6DLliuBc-QhpP2VinYnKTUOU7X3zG3PlLsbzRoIg130_assertion {
  miriam-gene:2064 a ncit:C16612 .
  
  lld:C0206701 a ncit:C7057 .
  
  dgn-gda:DGNfcd5f7b0061cb6b7522001128c88dc5e sio:SIO_000628 miriam-gene:2064, lld:C0206701;
    a sio:SIO_001121 .
}

dgn-np:NP884607.RASEn6DLliuBc-QhpP2VinYnKTUOU7X3zG3PlLsbzRoIg130_provenance {
  dgn-np:NP884607.RASEn6DLliuBc-QhpP2VinYnKTUOU7X3zG3PlLsbzRoIg130_assertion dcterms:description
      "[The purpose of this study was to examine the frequency and clinicopathological correlations of gene amplification, protein expression, and mutations of EGFR and ERBB2 in serous carcinoma, the most common and aggressive type of ovarian 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:16607561;
    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:NP884607.RASEn6DLliuBc-QhpP2VinYnKTUOU7X3zG3PlLsbzRoIg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:00+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" .
}