@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP315362.RAxNhoxAq9i0jOKrFyvdRebCa2r8Bba1lgFeVXtO3Xz3E> .
@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:NP315362.RAxNhoxAq9i0jOKrFyvdRebCa2r8Bba1lgFeVXtO3Xz3E130_head {
  this: np:hasAssertion dgn-np:NP315362.RAxNhoxAq9i0jOKrFyvdRebCa2r8Bba1lgFeVXtO3Xz3E130_assertion;
    np:hasProvenance dgn-np:NP315362.RAxNhoxAq9i0jOKrFyvdRebCa2r8Bba1lgFeVXtO3Xz3E130_provenance;
    np:hasPublicationInfo dgn-np:NP315362.RAxNhoxAq9i0jOKrFyvdRebCa2r8Bba1lgFeVXtO3Xz3E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP315362.RAxNhoxAq9i0jOKrFyvdRebCa2r8Bba1lgFeVXtO3Xz3E130_assertion a np:Assertion .
  
  dgn-np:NP315362.RAxNhoxAq9i0jOKrFyvdRebCa2r8Bba1lgFeVXtO3Xz3E130_provenance a np:Provenance .
  
  dgn-np:NP315362.RAxNhoxAq9i0jOKrFyvdRebCa2r8Bba1lgFeVXtO3Xz3E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP315362.RAxNhoxAq9i0jOKrFyvdRebCa2r8Bba1lgFeVXtO3Xz3E130_assertion {
  miriam-gene:1956 a ncit:C16612 .
  
  lld:C1140680 a ncit:C7057 .
  
  dgn-gda:DGNf0a571bc703aa70a55554888fc1dd00e sio:SIO_000628 miriam-gene:1956, lld:C1140680;
    a sio:SIO_001121 .
}

dgn-np:NP315362.RAxNhoxAq9i0jOKrFyvdRebCa2r8Bba1lgFeVXtO3Xz3E130_provenance {
  dgn-np:NP315362.RAxNhoxAq9i0jOKrFyvdRebCa2r8Bba1lgFeVXtO3Xz3E130_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:NP315362.RAxNhoxAq9i0jOKrFyvdRebCa2r8Bba1lgFeVXtO3Xz3E130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:00+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" .
}