@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP889035.RAzXsATBBZfSV58fh2TJTQ_OxIo0KC6_vNl4JceMO5vbE> .
@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:NP889035.RAzXsATBBZfSV58fh2TJTQ_OxIo0KC6_vNl4JceMO5vbE130_head {
  this: np:hasAssertion dgn-np:NP889035.RAzXsATBBZfSV58fh2TJTQ_OxIo0KC6_vNl4JceMO5vbE130_assertion;
    np:hasProvenance dgn-np:NP889035.RAzXsATBBZfSV58fh2TJTQ_OxIo0KC6_vNl4JceMO5vbE130_provenance;
    np:hasPublicationInfo dgn-np:NP889035.RAzXsATBBZfSV58fh2TJTQ_OxIo0KC6_vNl4JceMO5vbE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP889035.RAzXsATBBZfSV58fh2TJTQ_OxIo0KC6_vNl4JceMO5vbE130_assertion a np:Assertion .
  
  dgn-np:NP889035.RAzXsATBBZfSV58fh2TJTQ_OxIo0KC6_vNl4JceMO5vbE130_provenance a np:Provenance .
  
  dgn-np:NP889035.RAzXsATBBZfSV58fh2TJTQ_OxIo0KC6_vNl4JceMO5vbE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP889035.RAzXsATBBZfSV58fh2TJTQ_OxIo0KC6_vNl4JceMO5vbE130_assertion {
  miriam-gene:1436 a ncit:C16612 .
  
  lld:C0024299 a ncit:C7057 .
  
  dgn-gda:DGN5cabb1543cf8aa774f1f08b399fbfb5b sio:SIO_000628 miriam-gene:1436, lld:C0024299;
    a sio:SIO_001121 .
}

dgn-np:NP889035.RAzXsATBBZfSV58fh2TJTQ_OxIo0KC6_vNl4JceMO5vbE130_provenance {
  dgn-np:NP889035.RAzXsATBBZfSV58fh2TJTQ_OxIo0KC6_vNl4JceMO5vbE130_assertion dcterms:description
      "[Cases in point are the detection of RAS and FMS mutations in healthy individuals who had been treated in the past with cytotoxic therapy for lymphoma, the frequent observation of clonal remission in AML patients, or the identification of oncogene mutations in healthy individuals without even a history of malignancy or chemotherapy.]. 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:1613006;
    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:NP889035.RAzXsATBBZfSV58fh2TJTQ_OxIo0KC6_vNl4JceMO5vbE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:06+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" .
}