@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP349670.RAHS-KZiADd0jtTul4eZLWgPNWYcutrkJHKyWuKr_hRoo> .
@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:NP349670.RAHS-KZiADd0jtTul4eZLWgPNWYcutrkJHKyWuKr_hRoo130_head {
  this: np:hasAssertion dgn-np:NP349670.RAHS-KZiADd0jtTul4eZLWgPNWYcutrkJHKyWuKr_hRoo130_assertion;
    np:hasProvenance dgn-np:NP349670.RAHS-KZiADd0jtTul4eZLWgPNWYcutrkJHKyWuKr_hRoo130_provenance;
    np:hasPublicationInfo dgn-np:NP349670.RAHS-KZiADd0jtTul4eZLWgPNWYcutrkJHKyWuKr_hRoo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP349670.RAHS-KZiADd0jtTul4eZLWgPNWYcutrkJHKyWuKr_hRoo130_assertion a np:Assertion .
  
  dgn-np:NP349670.RAHS-KZiADd0jtTul4eZLWgPNWYcutrkJHKyWuKr_hRoo130_provenance a np:Provenance .
  
  dgn-np:NP349670.RAHS-KZiADd0jtTul4eZLWgPNWYcutrkJHKyWuKr_hRoo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP349670.RAHS-KZiADd0jtTul4eZLWgPNWYcutrkJHKyWuKr_hRoo130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0026499 a ncit:C7057 .
  
  dgn-gda:DGNf7b52a61a32827c9a8f27fec26fc2f80 sio:SIO_000628 miriam-gene:7157, lld:C0026499;
    a sio:SIO_001122 .
}

dgn-np:NP349670.RAHS-KZiADd0jtTul4eZLWgPNWYcutrkJHKyWuKr_hRoo130_provenance {
  dgn-np:NP349670.RAHS-KZiADd0jtTul4eZLWgPNWYcutrkJHKyWuKr_hRoo130_assertion dcterms:description
      "[Apart from the strong phenotypic impact of addition of acute myeloid leukemia/myelodysplasia-associated translocations and inversions, such as inv(3)(q21q26), t(3;21)(q26;q22), and t(15;17)(q22;q12-21), in CML BC, only a few significant differences between myeloid and lymphoid BC are discerned, with i(17q) and TP53 mutations being more common in myeloid BC and monosomy 7, hypodiploidy, and CDKN2A deletions being more frequent in lymphoid BC.]. 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:11919388;
    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:NP349670.RAHS-KZiADd0jtTul4eZLWgPNWYcutrkJHKyWuKr_hRoo130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:23+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" .
}