@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP340948.RAU1v5BlJJGKRcH6sOKnXimPMclI53TmR2k8sJrtALOxw> .
@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:NP340948.RAU1v5BlJJGKRcH6sOKnXimPMclI53TmR2k8sJrtALOxw130_head {
  this: np:hasAssertion dgn-np:NP340948.RAU1v5BlJJGKRcH6sOKnXimPMclI53TmR2k8sJrtALOxw130_assertion ;
    np:hasProvenance dgn-np:NP340948.RAU1v5BlJJGKRcH6sOKnXimPMclI53TmR2k8sJrtALOxw130_provenance ;
    np:hasPublicationInfo dgn-np:NP340948.RAU1v5BlJJGKRcH6sOKnXimPMclI53TmR2k8sJrtALOxw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP340948.RAU1v5BlJJGKRcH6sOKnXimPMclI53TmR2k8sJrtALOxw130_assertion a np:Assertion .
  dgn-np:NP340948.RAU1v5BlJJGKRcH6sOKnXimPMclI53TmR2k8sJrtALOxw130_provenance a np:Provenance .
  dgn-np:NP340948.RAU1v5BlJJGKRcH6sOKnXimPMclI53TmR2k8sJrtALOxw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP340948.RAU1v5BlJJGKRcH6sOKnXimPMclI53TmR2k8sJrtALOxw130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  lld:C3463824 a ncit:C7057 .
  dgn-gda:DGNbbe9938559c34d78ceb4372e14a23a94 sio:SIO_000628 miriam-gene:7157 , lld:C3463824 ;
    a sio:SIO_001121 .
}
dgn-np:NP340948.RAU1v5BlJJGKRcH6sOKnXimPMclI53TmR2k8sJrtALOxw130_provenance {
  dgn-np:NP340948.RAU1v5BlJJGKRcH6sOKnXimPMclI53TmR2k8sJrtALOxw130_assertion dcterms:description "[Increased incidence of p53 gene aberrations or chromosome 17p monosomy resulting from an isochromosome 17q [i(17q)] has been observed with transition of chronic myelogenous leukemia (CML) to myeloid blast crisis (BC), and in some patients with poor risk acute myeloid leukemia (AML) progressing from myelodysplastic syndrome (MDS).]. 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:8505851 ;
    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:NP340948.RAU1v5BlJJGKRcH6sOKnXimPMclI53TmR2k8sJrtALOxw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:20+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" .
}