@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP61162.RA4MWymq1lDFVMvC3psCizofkojjJf-or_Y711LxKuT88> .
@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:NP61162.RA4MWymq1lDFVMvC3psCizofkojjJf-or_Y711LxKuT88130_head {
  this: np:hasAssertion dgn-np:NP61162.RA4MWymq1lDFVMvC3psCizofkojjJf-or_Y711LxKuT88130_assertion;
    np:hasProvenance dgn-np:NP61162.RA4MWymq1lDFVMvC3psCizofkojjJf-or_Y711LxKuT88130_provenance;
    np:hasPublicationInfo dgn-np:NP61162.RA4MWymq1lDFVMvC3psCizofkojjJf-or_Y711LxKuT88130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP61162.RA4MWymq1lDFVMvC3psCizofkojjJf-or_Y711LxKuT88130_assertion a np:Assertion .
  
  dgn-np:NP61162.RA4MWymq1lDFVMvC3psCizofkojjJf-or_Y711LxKuT88130_provenance a np:Provenance .
  
  dgn-np:NP61162.RA4MWymq1lDFVMvC3psCizofkojjJf-or_Y711LxKuT88130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP61162.RA4MWymq1lDFVMvC3psCizofkojjJf-or_Y711LxKuT88130_assertion {
  miriam-gene:3845 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGN42839cee207f5bce11741dbe0a7cbe76 sio:SIO_000628 miriam-gene:3845, lld:C1527249;
    a sio:SIO_001122 .
}

dgn-np:NP61162.RA4MWymq1lDFVMvC3psCizofkojjJf-or_Y711LxKuT88130_provenance {
  dgn-np:NP61162.RA4MWymq1lDFVMvC3psCizofkojjJf-or_Y711LxKuT88130_assertion dcterms:description
      "[The study suggests that activating KRAS mutants is a particularly important independent predictive marker in mCRC patients treated with cetuximab plus chemotherapy, of which combing activating KRAS mutants and EGFR could help to identify the subgroup of patients who are most likely to respond to cetuximab plus chemotherapy.]. 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:20010090;
    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:NP61162.RA4MWymq1lDFVMvC3psCizofkojjJf-or_Y711LxKuT88130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:29+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" .
}