@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP705595.RAXIkNO_RCChf_qBAWNaxhEIeO7waI7LX9RA2HvxYhAB4> .
@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:NP705595.RAXIkNO_RCChf_qBAWNaxhEIeO7waI7LX9RA2HvxYhAB4130_head {
  this: np:hasAssertion dgn-np:NP705595.RAXIkNO_RCChf_qBAWNaxhEIeO7waI7LX9RA2HvxYhAB4130_assertion;
    np:hasProvenance dgn-np:NP705595.RAXIkNO_RCChf_qBAWNaxhEIeO7waI7LX9RA2HvxYhAB4130_provenance;
    np:hasPublicationInfo dgn-np:NP705595.RAXIkNO_RCChf_qBAWNaxhEIeO7waI7LX9RA2HvxYhAB4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP705595.RAXIkNO_RCChf_qBAWNaxhEIeO7waI7LX9RA2HvxYhAB4130_assertion a np:Assertion .
  
  dgn-np:NP705595.RAXIkNO_RCChf_qBAWNaxhEIeO7waI7LX9RA2HvxYhAB4130_provenance a np:Provenance .
  
  dgn-np:NP705595.RAXIkNO_RCChf_qBAWNaxhEIeO7waI7LX9RA2HvxYhAB4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP705595.RAXIkNO_RCChf_qBAWNaxhEIeO7waI7LX9RA2HvxYhAB4130_assertion {
  miriam-gene:238 a ncit:C16612 .
  
  lld:C0007131 a ncit:C7057 .
  
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dgn-np:NP705595.RAXIkNO_RCChf_qBAWNaxhEIeO7waI7LX9RA2HvxYhAB4130_provenance {
  dgn-np:NP705595.RAXIkNO_RCChf_qBAWNaxhEIeO7waI7LX9RA2HvxYhAB4130_assertion dcterms:description
      "[In the present review I summarize how detection of EML4-ALK cDNA may become a sensitive diagnostic means for NSCLC cases that are positive for the fusion gene, and discuss whether suppression of ALK enzymatic activity could be an effective treatment strategy against this intractable disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    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;
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}

dgn-np:NP705595.RAXIkNO_RCChf_qBAWNaxhEIeO7waI7LX9RA2HvxYhAB4130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:05+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}