@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP585927.RAq-h8T_n0QO0aQyYjUsi3djB8os_Lt53MQmhwU7G0agE> .
@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:NP585927.RAq-h8T_n0QO0aQyYjUsi3djB8os_Lt53MQmhwU7G0agE130_head {
  this: np:hasAssertion dgn-np:NP585927.RAq-h8T_n0QO0aQyYjUsi3djB8os_Lt53MQmhwU7G0agE130_assertion;
    np:hasProvenance dgn-np:NP585927.RAq-h8T_n0QO0aQyYjUsi3djB8os_Lt53MQmhwU7G0agE130_provenance;
    np:hasPublicationInfo dgn-np:NP585927.RAq-h8T_n0QO0aQyYjUsi3djB8os_Lt53MQmhwU7G0agE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP585927.RAq-h8T_n0QO0aQyYjUsi3djB8os_Lt53MQmhwU7G0agE130_assertion a np:Assertion .
  
  dgn-np:NP585927.RAq-h8T_n0QO0aQyYjUsi3djB8os_Lt53MQmhwU7G0agE130_provenance a np:Provenance .
  
  dgn-np:NP585927.RAq-h8T_n0QO0aQyYjUsi3djB8os_Lt53MQmhwU7G0agE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP585927.RAq-h8T_n0QO0aQyYjUsi3djB8os_Lt53MQmhwU7G0agE130_assertion {
  miriam-gene:1956 a ncit:C16612 .
  
  lld:C0242379 a ncit:C7057 .
  
  dgn-gda:DGNaa28cfebe8428da4636790474c9fe52f sio:SIO_000628 miriam-gene:1956, lld:C0242379;
    a sio:SIO_001121 .
}

dgn-np:NP585927.RAq-h8T_n0QO0aQyYjUsi3djB8os_Lt53MQmhwU7G0agE130_provenance {
  dgn-np:NP585927.RAq-h8T_n0QO0aQyYjUsi3djB8os_Lt53MQmhwU7G0agE130_assertion dcterms:description
      "[Two types of somatic mutations (in-frame deletions and point substitutions) in the EGFR gene were successfully identified within 3.5h using this system, suggesting that this system could be used in clinical tests of EGFR gene mutations in lung cancer, and potentially other cancer, patients.]. 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:17187977;
    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:NP585927.RAq-h8T_n0QO0aQyYjUsi3djB8os_Lt53MQmhwU7G0agE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:10+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" .
}