@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP660685.RAYzPEMk1caG2Z5Sd-SZ3HxvJ9CgDIPeSQSVDn7D0zj8Q> .
@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:NP660685.RAYzPEMk1caG2Z5Sd-SZ3HxvJ9CgDIPeSQSVDn7D0zj8Q130_head {
  this: np:hasAssertion dgn-np:NP660685.RAYzPEMk1caG2Z5Sd-SZ3HxvJ9CgDIPeSQSVDn7D0zj8Q130_assertion;
    np:hasProvenance dgn-np:NP660685.RAYzPEMk1caG2Z5Sd-SZ3HxvJ9CgDIPeSQSVDn7D0zj8Q130_provenance;
    np:hasPublicationInfo dgn-np:NP660685.RAYzPEMk1caG2Z5Sd-SZ3HxvJ9CgDIPeSQSVDn7D0zj8Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP660685.RAYzPEMk1caG2Z5Sd-SZ3HxvJ9CgDIPeSQSVDn7D0zj8Q130_assertion a np:Assertion .
  
  dgn-np:NP660685.RAYzPEMk1caG2Z5Sd-SZ3HxvJ9CgDIPeSQSVDn7D0zj8Q130_provenance a np:Provenance .
  
  dgn-np:NP660685.RAYzPEMk1caG2Z5Sd-SZ3HxvJ9CgDIPeSQSVDn7D0zj8Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP660685.RAYzPEMk1caG2Z5Sd-SZ3HxvJ9CgDIPeSQSVDn7D0zj8Q130_assertion {
  miriam-gene:4893 a ncit:C16612 .
  
  lld:C0023473 a ncit:C7057 .
  
  dgn-gda:DGN596241fef5145ddec86be478d55b5ea4 sio:SIO_000628 miriam-gene:4893, lld:C0023473;
    a sio:SIO_001121 .
}

dgn-np:NP660685.RAYzPEMk1caG2Z5Sd-SZ3HxvJ9CgDIPeSQSVDn7D0zj8Q130_provenance {
  dgn-np:NP660685.RAYzPEMk1caG2Z5Sd-SZ3HxvJ9CgDIPeSQSVDn7D0zj8Q130_assertion dcterms:description
      "[Using the polymerase chain reaction-single strand conformation polymorphism method and direct sequencing, 12 acute myeloid leukemia (AML) cell lines and 108 fresh childhood myeloid tumor specimens, including 67 AML, 29 myelodysplastic syndrome (MDS), and 12 juvenile chronic myelocytic leukemia (JCML) were examined for mutation in H-, K-, and N-RAS genes.]. 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:9379676;
    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:NP660685.RAYzPEMk1caG2Z5Sd-SZ3HxvJ9CgDIPeSQSVDn7D0zj8Q130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:39+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" .
}