@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP878008.RAzUy2FlmMFKwGCMoRWCjk_4wFdM68dnIg76miUPr5Gps> .
@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:NP878008.RAzUy2FlmMFKwGCMoRWCjk_4wFdM68dnIg76miUPr5Gps130_head {
  this: np:hasAssertion dgn-np:NP878008.RAzUy2FlmMFKwGCMoRWCjk_4wFdM68dnIg76miUPr5Gps130_assertion;
    np:hasProvenance dgn-np:NP878008.RAzUy2FlmMFKwGCMoRWCjk_4wFdM68dnIg76miUPr5Gps130_provenance;
    np:hasPublicationInfo dgn-np:NP878008.RAzUy2FlmMFKwGCMoRWCjk_4wFdM68dnIg76miUPr5Gps130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP878008.RAzUy2FlmMFKwGCMoRWCjk_4wFdM68dnIg76miUPr5Gps130_assertion a np:Assertion .
  
  dgn-np:NP878008.RAzUy2FlmMFKwGCMoRWCjk_4wFdM68dnIg76miUPr5Gps130_provenance a np:Provenance .
  
  dgn-np:NP878008.RAzUy2FlmMFKwGCMoRWCjk_4wFdM68dnIg76miUPr5Gps130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP878008.RAzUy2FlmMFKwGCMoRWCjk_4wFdM68dnIg76miUPr5Gps130_assertion {
  miriam-gene:3918 a ncit:C16612 .
  
  lld:C0684249 a ncit:C7057 .
  
  dgn-gda:DGN41ae2eb354c417904ab4932966ddc571 sio:SIO_000628 miriam-gene:3918, lld:C0684249;
    a sio:SIO_001121 .
}

dgn-np:NP878008.RAzUy2FlmMFKwGCMoRWCjk_4wFdM68dnIg76miUPr5Gps130_provenance {
  dgn-np:NP878008.RAzUy2FlmMFKwGCMoRWCjk_4wFdM68dnIg76miUPr5Gps130_assertion dcterms:description
      "[Polymerase chain reaction detection of epithelial growth factor receptor (EGFR) mutations in cerebrospinal fluid (CSF), which are predictive markers for EGFR tyrosine kinase inhibitor therapy in lung cancer, might be important to diagnose and to treat NM in patients with 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:21610522;
    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:NP878008.RAzUy2FlmMFKwGCMoRWCjk_4wFdM68dnIg76miUPr5Gps130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:56+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" .
}