@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP453068.RATv64tsF4uvXXDIurx5wKMz9NhKL4_JqGfZEqgnavQ90> .
@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:NP453068.RATv64tsF4uvXXDIurx5wKMz9NhKL4_JqGfZEqgnavQ90130_head {
  this: np:hasAssertion dgn-np:NP453068.RATv64tsF4uvXXDIurx5wKMz9NhKL4_JqGfZEqgnavQ90130_assertion;
    np:hasProvenance dgn-np:NP453068.RATv64tsF4uvXXDIurx5wKMz9NhKL4_JqGfZEqgnavQ90130_provenance;
    np:hasPublicationInfo dgn-np:NP453068.RATv64tsF4uvXXDIurx5wKMz9NhKL4_JqGfZEqgnavQ90130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP453068.RATv64tsF4uvXXDIurx5wKMz9NhKL4_JqGfZEqgnavQ90130_assertion a np:Assertion .
  
  dgn-np:NP453068.RATv64tsF4uvXXDIurx5wKMz9NhKL4_JqGfZEqgnavQ90130_provenance a np:Provenance .
  
  dgn-np:NP453068.RATv64tsF4uvXXDIurx5wKMz9NhKL4_JqGfZEqgnavQ90130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP453068.RATv64tsF4uvXXDIurx5wKMz9NhKL4_JqGfZEqgnavQ90130_assertion {
  miriam-gene:5156 a ncit:C16612 .
  
  lld:C0677936 a ncit:C7057 .
  
  dgn-gda:DGN5051da606143fe1aea62401b882b55df sio:SIO_000628 miriam-gene:5156, lld:C0677936;
    a sio:SIO_001121 .
}

dgn-np:NP453068.RATv64tsF4uvXXDIurx5wKMz9NhKL4_JqGfZEqgnavQ90130_provenance {
  dgn-np:NP453068.RATv64tsF4uvXXDIurx5wKMz9NhKL4_JqGfZEqgnavQ90130_assertion dcterms:description
      "[The low frequency of clinical resistance to PDGFR inhibitors in myeloid neoplasms with abnormalities of PDGFRA might be related to the limited repertoire of possible PDGFRA kinase domain mutations in vitro.]. 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:20972453;
    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:NP453068.RATv64tsF4uvXXDIurx5wKMz9NhKL4_JqGfZEqgnavQ90130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:30+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" .
}