@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng> .
@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:NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_head {
  this: np:hasAssertion dgn-np:NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_assertion;
    np:hasProvenance dgn-np:NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_provenance;
    np:hasPublicationInfo dgn-np:NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_assertion a np:Assertion .
  
  dgn-np:NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_provenance a np:Provenance .
  
  dgn-np:NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_assertion {
  miriam-gene:3265 a ncit:C16612 .
  
  lld:C0023467 a ncit:C7057 .
  
  dgn-gda:DGN89c11952313bfe93d2d2159a3c717e67 sio:SIO_000628 miriam-gene:3265, lld:C0023467;
    a sio:SIO_001121 .
}

dgn-np:NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_provenance {
  dgn-np:NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_assertion dcterms:description
      "[Mutations at codon 12, 13, and 61 of the HRAS, KRAS, and NRAS genes were evaluated in 99 cases of pediatric acute myeloid leukemia (AML) using oligonucleotide hybridization to polymerase chain reacted derived products.]. 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:2278970;
    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:NP300337.RABn6eEzrcaE89QdNN-kM4662ogb5-Dri0rOq4HROdXng130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:50+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" .
}