@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP598685.RAM_eVx2ktgauzdtF3P5LVb7UM_Cx_bocevgJxoyu9T1c> .
@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/v3.0.0/void/> .

dgn-np:NP598685.RAM_eVx2ktgauzdtF3P5LVb7UM_Cx_bocevgJxoyu9T1c130_head {
  this: np:hasAssertion dgn-np:NP598685.RAM_eVx2ktgauzdtF3P5LVb7UM_Cx_bocevgJxoyu9T1c130_assertion;
    np:hasProvenance dgn-np:NP598685.RAM_eVx2ktgauzdtF3P5LVb7UM_Cx_bocevgJxoyu9T1c130_provenance;
    np:hasPublicationInfo dgn-np:NP598685.RAM_eVx2ktgauzdtF3P5LVb7UM_Cx_bocevgJxoyu9T1c130_publicationInfo;
    a np:Nanopublication .
  
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      np:PublicationInfo .
}

dgn-np:NP598685.RAM_eVx2ktgauzdtF3P5LVb7UM_Cx_bocevgJxoyu9T1c130_assertion {
  miriam-gene:4893 a ncit:C16612 .
  
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dgn-np:NP598685.RAM_eVx2ktgauzdtF3P5LVb7UM_Cx_bocevgJxoyu9T1c130_provenance {
  dgn-np:NP598685.RAM_eVx2ktgauzdtF3P5LVb7UM_Cx_bocevgJxoyu9T1c130_assertion dcterms:description
      "[These results indicate the following: (i) RAS oncogenes are not found in all types of human malignancies, (ii) significant differences in the frequency of RAS mutations can be found among subtypes of neoplasms derived from the same tissue, (iii) in lymphoid neoplasms the NRAS mutation correlates with the most undifferentiated acute lymphocytic leukemia phenotype, and (iv) NRAS mutations present in only a fraction of malignant cells may result from either the selective loss or the acquisition of mutated alleles during tumor development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
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  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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 .
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dgn-np:NP598685.RAM_eVx2ktgauzdtF3P5LVb7UM_Cx_bocevgJxoyu9T1c130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:38+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
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