@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP222361.RAAFjDovRg8seqINOzLfSqOQS7_eQjJZgjV9C8k1JAI2Y> .
@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:NP222361.RAAFjDovRg8seqINOzLfSqOQS7_eQjJZgjV9C8k1JAI2Y130_head {
  this: np:hasAssertion dgn-np:NP222361.RAAFjDovRg8seqINOzLfSqOQS7_eQjJZgjV9C8k1JAI2Y130_assertion;
    np:hasProvenance dgn-np:NP222361.RAAFjDovRg8seqINOzLfSqOQS7_eQjJZgjV9C8k1JAI2Y130_provenance;
    np:hasPublicationInfo dgn-np:NP222361.RAAFjDovRg8seqINOzLfSqOQS7_eQjJZgjV9C8k1JAI2Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP222361.RAAFjDovRg8seqINOzLfSqOQS7_eQjJZgjV9C8k1JAI2Y130_assertion a np:Assertion .
  
  dgn-np:NP222361.RAAFjDovRg8seqINOzLfSqOQS7_eQjJZgjV9C8k1JAI2Y130_provenance a np:Provenance .
  
  dgn-np:NP222361.RAAFjDovRg8seqINOzLfSqOQS7_eQjJZgjV9C8k1JAI2Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP222361.RAAFjDovRg8seqINOzLfSqOQS7_eQjJZgjV9C8k1JAI2Y130_assertion {
  miriam-gene:238 a ncit:C16612 .
  
  lld:C0001418 a ncit:C7057 .
  
  dgn-gda:DGN698c4a93ea8e0cd397f75179f7ece45a sio:SIO_000628 miriam-gene:238, lld:C0001418;
    a sio:SIO_001121 .
}

dgn-np:NP222361.RAAFjDovRg8seqINOzLfSqOQS7_eQjJZgjV9C8k1JAI2Y130_provenance {
  dgn-np:NP222361.RAAFjDovRg8seqINOzLfSqOQS7_eQjJZgjV9C8k1JAI2Y130_assertion dcterms:description
      "[The major recommendations are to use testing for EGFR mutations and ALK fusions to guide patient selection for therapy with an epidermal growth factor receptor (EGFR) or anaplastic lymphoma kinase (ALK) inhibitor, respectively, in all patients with advanced-stage adenocarcinoma, regardless of sex, race, smoking history, or other clinical risk factors, and to prioritize EGFR and ALK testing over other molecular predictive tests.]. 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:23551194;
    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:NP222361.RAAFjDovRg8seqINOzLfSqOQS7_eQjJZgjV9C8k1JAI2Y130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:03+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" .
}