@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP501100.RADpcD88B11kvv0v5LOcKkvyrnpqxf_BJVvvaAu-hlMKU> .
@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:NP501100.RADpcD88B11kvv0v5LOcKkvyrnpqxf_BJVvvaAu-hlMKU130_head {
  this: np:hasAssertion dgn-np:NP501100.RADpcD88B11kvv0v5LOcKkvyrnpqxf_BJVvvaAu-hlMKU130_assertion;
    np:hasProvenance dgn-np:NP501100.RADpcD88B11kvv0v5LOcKkvyrnpqxf_BJVvvaAu-hlMKU130_provenance;
    np:hasPublicationInfo dgn-np:NP501100.RADpcD88B11kvv0v5LOcKkvyrnpqxf_BJVvvaAu-hlMKU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP501100.RADpcD88B11kvv0v5LOcKkvyrnpqxf_BJVvvaAu-hlMKU130_assertion a np:Assertion .
  
  dgn-np:NP501100.RADpcD88B11kvv0v5LOcKkvyrnpqxf_BJVvvaAu-hlMKU130_provenance a np:Provenance .
  
  dgn-np:NP501100.RADpcD88B11kvv0v5LOcKkvyrnpqxf_BJVvvaAu-hlMKU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP501100.RADpcD88B11kvv0v5LOcKkvyrnpqxf_BJVvvaAu-hlMKU130_assertion {
  miriam-gene:5156 a ncit:C16612 .
  
  lld:C0027627 a ncit:C7057 .
  
  dgn-gda:DGNb42e7b1a681297656684e18047338b29 sio:SIO_000628 miriam-gene:5156, lld:C0027627;
    a sio:SIO_001121 .
}

dgn-np:NP501100.RADpcD88B11kvv0v5LOcKkvyrnpqxf_BJVvvaAu-hlMKU130_provenance {
  dgn-np:NP501100.RADpcD88B11kvv0v5LOcKkvyrnpqxf_BJVvvaAu-hlMKU130_assertion dcterms:description
      "[Gene mutations of KIT or PDGFRA are critical in GISTs, because the aberrant versions not only are correlated with the specific cell morphology, histologic phenotype, metastasis, and prognosis, but also are the targets of therapy with imatinib and other agents.]. 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:18671247;
    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:NP501100.RADpcD88B11kvv0v5LOcKkvyrnpqxf_BJVvvaAu-hlMKU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:58+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" .
}