@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP598673.RAhWUZQTsNhdRWs8L2uqESXdl9riFZyR6a8bwbjliEJ7c> .
@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:NP598673.RAhWUZQTsNhdRWs8L2uqESXdl9riFZyR6a8bwbjliEJ7c130_head {
  this: np:hasAssertion dgn-np:NP598673.RAhWUZQTsNhdRWs8L2uqESXdl9riFZyR6a8bwbjliEJ7c130_assertion;
    np:hasProvenance dgn-np:NP598673.RAhWUZQTsNhdRWs8L2uqESXdl9riFZyR6a8bwbjliEJ7c130_provenance;
    np:hasPublicationInfo dgn-np:NP598673.RAhWUZQTsNhdRWs8L2uqESXdl9riFZyR6a8bwbjliEJ7c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP598673.RAhWUZQTsNhdRWs8L2uqESXdl9riFZyR6a8bwbjliEJ7c130_assertion a np:Assertion .
  
  dgn-np:NP598673.RAhWUZQTsNhdRWs8L2uqESXdl9riFZyR6a8bwbjliEJ7c130_provenance a np:Provenance .
  
  dgn-np:NP598673.RAhWUZQTsNhdRWs8L2uqESXdl9riFZyR6a8bwbjliEJ7c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP598673.RAhWUZQTsNhdRWs8L2uqESXdl9riFZyR6a8bwbjliEJ7c130_assertion {
  miriam-gene:4893 a ncit:C16612 .
  
  lld:C0026986 a ncit:C7057 .
  
  dgn-gda:DGN0f9fcee8898e17308c4758c72267aaa1 sio:SIO_000628 miriam-gene:4893, lld:C0026986;
    a sio:SIO_001121 .
}

dgn-np:NP598673.RAhWUZQTsNhdRWs8L2uqESXdl9riFZyR6a8bwbjliEJ7c130_provenance {
  dgn-np:NP598673.RAhWUZQTsNhdRWs8L2uqESXdl9riFZyR6a8bwbjliEJ7c130_assertion dcterms:description
      "[In addition to the detection of mutations known to be associated with MDS in NRAS, KRAS, MPL, NPM1, IDH1, PTPN11, APC and MET, single nucleotide variants so far unrelated to MDS in STK11 (n=1), KDR (n=3), ATM (n=1) and JAK3 (n=2) were identified.]. 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:24674452;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  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 .
}

dgn-np:NP598673.RAhWUZQTsNhdRWs8L2uqESXdl9riFZyR6a8bwbjliEJ7c130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:38+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}