@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP598541.RAlVVRW6t9ar1-ncYbt5EM6tkLimbNtF3kkeV7OtqIK7I> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP598541.RAlVVRW6t9ar1-ncYbt5EM6tkLimbNtF3kkeV7OtqIK7I130_head {
  this: np:hasAssertion dgn-np:NP598541.RAlVVRW6t9ar1-ncYbt5EM6tkLimbNtF3kkeV7OtqIK7I130_assertion;
    np:hasProvenance dgn-np:NP598541.RAlVVRW6t9ar1-ncYbt5EM6tkLimbNtF3kkeV7OtqIK7I130_provenance;
    np:hasPublicationInfo dgn-np:NP598541.RAlVVRW6t9ar1-ncYbt5EM6tkLimbNtF3kkeV7OtqIK7I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP598541.RAlVVRW6t9ar1-ncYbt5EM6tkLimbNtF3kkeV7OtqIK7I130_assertion a np:Assertion .
  
  dgn-np:NP598541.RAlVVRW6t9ar1-ncYbt5EM6tkLimbNtF3kkeV7OtqIK7I130_provenance a np:Provenance .
  
  dgn-np:NP598541.RAlVVRW6t9ar1-ncYbt5EM6tkLimbNtF3kkeV7OtqIK7I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP598541.RAlVVRW6t9ar1-ncYbt5EM6tkLimbNtF3kkeV7OtqIK7I130_assertion {
  miriam-gene:1956 a ncit:C16612 .
  
  lld:C0007131 a ncit:C7057 .
  
  dgn-gda:DGN738d8473a1ae30feec643d94d35541a5 sio:SIO_000628 miriam-gene:1956, lld:C0007131;
    a sio:SIO_001121 .
}

dgn-np:NP598541.RAlVVRW6t9ar1-ncYbt5EM6tkLimbNtF3kkeV7OtqIK7I130_provenance {
  dgn-np:NP598541.RAlVVRW6t9ar1-ncYbt5EM6tkLimbNtF3kkeV7OtqIK7I130_assertion dcterms:description
      "[In vitro analysis of NSCLC cells with endogenous EGFR mutations, recombinant expression of EGFR variants by transfection of several cell lines and the generation of transgenic mice expressing mutant EGFR were applied to study the impact of these genetic alterations on cellular signaling and cell fate.]. 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:17353898;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP598541.RAlVVRW6t9ar1-ncYbt5EM6tkLimbNtF3kkeV7OtqIK7I130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:17+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}