@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1011211.RAcKZ6NSOH7hTUfy_UFa7MgTOaWWfqg2MRIMLjaAPl35Y> .
@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:NP1011211.RAcKZ6NSOH7hTUfy_UFa7MgTOaWWfqg2MRIMLjaAPl35Y130_head {
  this: np:hasAssertion dgn-np:NP1011211.RAcKZ6NSOH7hTUfy_UFa7MgTOaWWfqg2MRIMLjaAPl35Y130_assertion;
    np:hasProvenance dgn-np:NP1011211.RAcKZ6NSOH7hTUfy_UFa7MgTOaWWfqg2MRIMLjaAPl35Y130_provenance;
    np:hasPublicationInfo dgn-np:NP1011211.RAcKZ6NSOH7hTUfy_UFa7MgTOaWWfqg2MRIMLjaAPl35Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1011211.RAcKZ6NSOH7hTUfy_UFa7MgTOaWWfqg2MRIMLjaAPl35Y130_assertion a np:Assertion .
  
  dgn-np:NP1011211.RAcKZ6NSOH7hTUfy_UFa7MgTOaWWfqg2MRIMLjaAPl35Y130_provenance a np:Provenance .
  
  dgn-np:NP1011211.RAcKZ6NSOH7hTUfy_UFa7MgTOaWWfqg2MRIMLjaAPl35Y130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1011211.RAcKZ6NSOH7hTUfy_UFa7MgTOaWWfqg2MRIMLjaAPl35Y130_assertion {
  miriam-gene:1956 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGN593dc60b7ac14216fbe73572b61925e5 sio:SIO_000628 miriam-gene:1956, lld:C0006142;
    a sio:SIO_001121 .
}

dgn-np:NP1011211.RAcKZ6NSOH7hTUfy_UFa7MgTOaWWfqg2MRIMLjaAPl35Y130_provenance {
  dgn-np:NP1011211.RAcKZ6NSOH7hTUfy_UFa7MgTOaWWfqg2MRIMLjaAPl35Y130_assertion dcterms:description
      "[Cancers with specific genetic abnormalities, for instance epidermal growth factor receptor (EGFR) mutant lung cancers and HER2 amplified breast cancers, are often sensitive to these new targeted therapies that can specifically inhibit the function of EGFR or HER2.]. 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:22959036;
    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:NP1011211.RAcKZ6NSOH7hTUfy_UFa7MgTOaWWfqg2MRIMLjaAPl35Y130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:24+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" .
}