@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP398155.RA7SzJ6RrlzBMaAawvToNix7h4JYXgYids2I_leI3NVWs> .
@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:NP398155.RA7SzJ6RrlzBMaAawvToNix7h4JYXgYids2I_leI3NVWs130_head {
  this: np:hasAssertion dgn-np:NP398155.RA7SzJ6RrlzBMaAawvToNix7h4JYXgYids2I_leI3NVWs130_assertion ;
    np:hasProvenance dgn-np:NP398155.RA7SzJ6RrlzBMaAawvToNix7h4JYXgYids2I_leI3NVWs130_provenance ;
    np:hasPublicationInfo dgn-np:NP398155.RA7SzJ6RrlzBMaAawvToNix7h4JYXgYids2I_leI3NVWs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP398155.RA7SzJ6RrlzBMaAawvToNix7h4JYXgYids2I_leI3NVWs130_assertion a np:Assertion .
  dgn-np:NP398155.RA7SzJ6RrlzBMaAawvToNix7h4JYXgYids2I_leI3NVWs130_provenance a np:Provenance .
  dgn-np:NP398155.RA7SzJ6RrlzBMaAawvToNix7h4JYXgYids2I_leI3NVWs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP398155.RA7SzJ6RrlzBMaAawvToNix7h4JYXgYids2I_leI3NVWs130_assertion {
  miriam-gene:1956 a ncit:C16612 .
  lld:C0085281 a ncit:C7057 .
  dgn-gda:DGN5ef2cd43fffa787da33c6764dcc855fd sio:SIO_000628 miriam-gene:1956 , lld:C0085281 ;
    a sio:SIO_001121 .
}
dgn-np:NP398155.RA7SzJ6RrlzBMaAawvToNix7h4JYXgYids2I_leI3NVWs130_provenance {
  dgn-np:NP398155.RA7SzJ6RrlzBMaAawvToNix7h4JYXgYids2I_leI3NVWs130_assertion dcterms:description "[Here, we combine carefully titrated lentiviral-mediated short hairpin RNA knockdown of the epidermal growth factor receptor (EGFR) with heterologous reconstitution by EGFR mutants to rigorously analyze the structural features and signaling activities that determine addiction to the mutationally activated EGFR in human lung cancer cells.]. 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:18711136 ;
    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:NP398155.RA7SzJ6RrlzBMaAawvToNix7h4JYXgYids2I_leI3NVWs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:57+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> ;
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}