@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP708789.RAmM2TZjdKsaQ68WnkqGVtvXBDybHtotiNLVOGYdUlKhQ> .
@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:NP708789.RAmM2TZjdKsaQ68WnkqGVtvXBDybHtotiNLVOGYdUlKhQ130_head {
  this: np:hasAssertion dgn-np:NP708789.RAmM2TZjdKsaQ68WnkqGVtvXBDybHtotiNLVOGYdUlKhQ130_assertion;
    np:hasProvenance dgn-np:NP708789.RAmM2TZjdKsaQ68WnkqGVtvXBDybHtotiNLVOGYdUlKhQ130_provenance;
    np:hasPublicationInfo dgn-np:NP708789.RAmM2TZjdKsaQ68WnkqGVtvXBDybHtotiNLVOGYdUlKhQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP708789.RAmM2TZjdKsaQ68WnkqGVtvXBDybHtotiNLVOGYdUlKhQ130_assertion a np:Assertion .
  
  dgn-np:NP708789.RAmM2TZjdKsaQ68WnkqGVtvXBDybHtotiNLVOGYdUlKhQ130_provenance a np:Provenance .
  
  dgn-np:NP708789.RAmM2TZjdKsaQ68WnkqGVtvXBDybHtotiNLVOGYdUlKhQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP708789.RAmM2TZjdKsaQ68WnkqGVtvXBDybHtotiNLVOGYdUlKhQ130_assertion {
  miriam-gene:3265 a ncit:C16612 .
  
  lld:C0023467 a ncit:C7057 .
  
  dgn-gda:DGNeee3f891567b84f29f4f0888d6ac0ed4 sio:SIO_000628 miriam-gene:3265, lld:C0023467;
    a sio:SIO_001121 .
}

dgn-np:NP708789.RAmM2TZjdKsaQ68WnkqGVtvXBDybHtotiNLVOGYdUlKhQ130_provenance {
  dgn-np:NP708789.RAmM2TZjdKsaQ68WnkqGVtvXBDybHtotiNLVOGYdUlKhQ130_assertion dcterms:description
      "[To search for additional, novel RAS mutations, we sequenced all coding exons in NRAS, KRAS, and HRAS in 329 acute myeloid leukemia (AML) patients, 32 chronic myelomonocytic leukemia (CMML) patients, and 96 healthy individuals.]. 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:19075190;
    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:NP708789.RAmM2TZjdKsaQ68WnkqGVtvXBDybHtotiNLVOGYdUlKhQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:06+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: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" .
}