@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP463815.RAbKB44f4Wy1JTh3ECVb8di12nQ6wZrgBX1oEXWW6ujbo> .
@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:NP463815.RAbKB44f4Wy1JTh3ECVb8di12nQ6wZrgBX1oEXWW6ujbo130_head {
  this: np:hasAssertion dgn-np:NP463815.RAbKB44f4Wy1JTh3ECVb8di12nQ6wZrgBX1oEXWW6ujbo130_assertion;
    np:hasProvenance dgn-np:NP463815.RAbKB44f4Wy1JTh3ECVb8di12nQ6wZrgBX1oEXWW6ujbo130_provenance;
    np:hasPublicationInfo dgn-np:NP463815.RAbKB44f4Wy1JTh3ECVb8di12nQ6wZrgBX1oEXWW6ujbo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP463815.RAbKB44f4Wy1JTh3ECVb8di12nQ6wZrgBX1oEXWW6ujbo130_assertion a np:Assertion .
  
  dgn-np:NP463815.RAbKB44f4Wy1JTh3ECVb8di12nQ6wZrgBX1oEXWW6ujbo130_provenance a np:Provenance .
  
  dgn-np:NP463815.RAbKB44f4Wy1JTh3ECVb8di12nQ6wZrgBX1oEXWW6ujbo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP463815.RAbKB44f4Wy1JTh3ECVb8di12nQ6wZrgBX1oEXWW6ujbo130_assertion {
  miriam-gene:4893 a ncit:C16612 .
  
  lld:C0026986 a ncit:C7057 .
  
  dgn-gda:DGN88d7b23f6f42a1b4512ab2b991f95ef7 sio:SIO_000628 miriam-gene:4893, lld:C0026986;
    a sio:SIO_001121 .
}

dgn-np:NP463815.RAbKB44f4Wy1JTh3ECVb8di12nQ6wZrgBX1oEXWW6ujbo130_provenance {
  dgn-np:NP463815.RAbKB44f4Wy1JTh3ECVb8di12nQ6wZrgBX1oEXWW6ujbo130_assertion dcterms:description
      "[Mutations of the NRAS and TP53 genes and internal tandem duplication (ITD) of the FLT3 gene are among the most frequently observed molecular abnormalities in the myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML).]. 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:15257941;
    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:NP463815.RAbKB44f4Wy1JTh3ECVb8di12nQ6wZrgBX1oEXWW6ujbo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:36+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" .
}