@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP74995.RAZLLEl0CAC-TCNRurdqk-9FQj6nrynA13M7alTqR4ASA> .
@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:NP74995.RAZLLEl0CAC-TCNRurdqk-9FQj6nrynA13M7alTqR4ASA130_head {
  this: np:hasAssertion dgn-np:NP74995.RAZLLEl0CAC-TCNRurdqk-9FQj6nrynA13M7alTqR4ASA130_assertion;
    np:hasProvenance dgn-np:NP74995.RAZLLEl0CAC-TCNRurdqk-9FQj6nrynA13M7alTqR4ASA130_provenance;
    np:hasPublicationInfo dgn-np:NP74995.RAZLLEl0CAC-TCNRurdqk-9FQj6nrynA13M7alTqR4ASA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP74995.RAZLLEl0CAC-TCNRurdqk-9FQj6nrynA13M7alTqR4ASA130_assertion a np:Assertion .
  
  dgn-np:NP74995.RAZLLEl0CAC-TCNRurdqk-9FQj6nrynA13M7alTqR4ASA130_provenance a np:Provenance .
  
  dgn-np:NP74995.RAZLLEl0CAC-TCNRurdqk-9FQj6nrynA13M7alTqR4ASA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP74995.RAZLLEl0CAC-TCNRurdqk-9FQj6nrynA13M7alTqR4ASA130_assertion {
  miriam-gene:2214 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGN105ce4ff77e4226bd24c0a2449660572 sio:SIO_000628 miriam-gene:2214, lld:C1527249;
    a sio:SIO_001122 .
}

dgn-np:NP74995.RAZLLEl0CAC-TCNRurdqk-9FQj6nrynA13M7alTqR4ASA130_provenance {
  dgn-np:NP74995.RAZLLEl0CAC-TCNRurdqk-9FQj6nrynA13M7alTqR4ASA130_assertion dcterms:description
      "[Intratumoral gene expression levels of EGFR, VEGFR2 and NRP as well as polymorphisms in FCGR3A, CyclinD1 and EGFR could predict clinical outcome in mCRC patients enrolled in BOND2, independent of KRAS mutation status.]. 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:21036743;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP74995.RAZLLEl0CAC-TCNRurdqk-9FQj6nrynA13M7alTqR4ASA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:36+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" .
}