@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP404208.RA_Yd-qF4kiTK-sxLJj3Q85voDPK8IFRol84cMuQjHN18> .
@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/v4.0.0/void/> .

dgn-np:NP404208.RA_Yd-qF4kiTK-sxLJj3Q85voDPK8IFRol84cMuQjHN18130_head {
  this: np:hasAssertion dgn-np:NP404208.RA_Yd-qF4kiTK-sxLJj3Q85voDPK8IFRol84cMuQjHN18130_assertion;
    np:hasProvenance dgn-np:NP404208.RA_Yd-qF4kiTK-sxLJj3Q85voDPK8IFRol84cMuQjHN18130_provenance;
    np:hasPublicationInfo dgn-np:NP404208.RA_Yd-qF4kiTK-sxLJj3Q85voDPK8IFRol84cMuQjHN18130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP404208.RA_Yd-qF4kiTK-sxLJj3Q85voDPK8IFRol84cMuQjHN18130_assertion a np:Assertion .
  
  dgn-np:NP404208.RA_Yd-qF4kiTK-sxLJj3Q85voDPK8IFRol84cMuQjHN18130_provenance a np:Provenance .
  
  dgn-np:NP404208.RA_Yd-qF4kiTK-sxLJj3Q85voDPK8IFRol84cMuQjHN18130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP404208.RA_Yd-qF4kiTK-sxLJj3Q85voDPK8IFRol84cMuQjHN18130_assertion {
  miriam-gene:171023 a ncit:C16612 .
  
  lld:C0033027 a ncit:C7057 .
  
  dgn-gda:DGNe7bfc92eafcb312065551cf931f4bcb0 sio:SIO_000628 miriam-gene:171023, lld:C0033027;
    a sio:SIO_001121 .
}

dgn-np:NP404208.RA_Yd-qF4kiTK-sxLJj3Q85voDPK8IFRol84cMuQjHN18130_provenance {
  dgn-np:NP404208.RA_Yd-qF4kiTK-sxLJj3Q85voDPK8IFRol84cMuQjHN18130_assertion dcterms:description
      "[Acquisition of the Philadelphia chromosome is an infrequent event in myelodysplastic syndrome, and the addition of this change to the initial genetic abnormality that caused MDS may have been associated with the accelerated clinical course of this patient.]. 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:12898186;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP404208.RA_Yd-qF4kiTK-sxLJj3Q85voDPK8IFRol84cMuQjHN18130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:48+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}