@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP353986.RA6EHqbVkLoGRV2HkO_Dp4y1cTSQl9oCWpYYHLOUyTQ2s> .
@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:NP353986.RA6EHqbVkLoGRV2HkO_Dp4y1cTSQl9oCWpYYHLOUyTQ2s130_head {
   this: np:hasAssertion dgn-np:NP353986.RA6EHqbVkLoGRV2HkO_Dp4y1cTSQl9oCWpYYHLOUyTQ2s130_assertion ;
    np:hasProvenance dgn-np:NP353986.RA6EHqbVkLoGRV2HkO_Dp4y1cTSQl9oCWpYYHLOUyTQ2s130_provenance ;
    np:hasPublicationInfo dgn-np:NP353986.RA6EHqbVkLoGRV2HkO_Dp4y1cTSQl9oCWpYYHLOUyTQ2s130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP353986.RA6EHqbVkLoGRV2HkO_Dp4y1cTSQl9oCWpYYHLOUyTQ2s130_assertion a np:Assertion .
  dgn-np:NP353986.RA6EHqbVkLoGRV2HkO_Dp4y1cTSQl9oCWpYYHLOUyTQ2s130_provenance a np:Provenance .
  dgn-np:NP353986.RA6EHqbVkLoGRV2HkO_Dp4y1cTSQl9oCWpYYHLOUyTQ2s130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP353986.RA6EHqbVkLoGRV2HkO_Dp4y1cTSQl9oCWpYYHLOUyTQ2s130_assertion {
   miriam-gene:4580 a ncit:C16612 .
  lld:C0023467 a ncit:C7057 .
  dgn-gda:DGNb3ddd153026569a40c4558af6b91481e sio:SIO_000628 miriam-gene:4580 , lld:C0023467 ;
    a sio:SIO_001121 .
}
dgn-np:NP353986.RA6EHqbVkLoGRV2HkO_Dp4y1cTSQl9oCWpYYHLOUyTQ2s130_provenance {
   dgn-np:NP353986.RA6EHqbVkLoGRV2HkO_Dp4y1cTSQl9oCWpYYHLOUyTQ2s130_assertion dcterms:description "[A combined bromodeoxyuridine (BrdU) and actinomycin D (AMD) treatment of methotrexate (MTX) synchronized bone marrow cells from four patients with chronic myelogenous leukemia (CML), and two each with acute lymphocytic (ALL) and acute nonlymphocytic (ANLL) leukemia were used to define the breakpoints involved in the t(9;22) found in subgroups of these three disorders.]. 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:6584200 ;
    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:NP353986.RA6EHqbVkLoGRV2HkO_Dp4y1cTSQl9oCWpYYHLOUyTQ2s130_publicationInfo {
   this: dcterms:created "2014-10-02T12:35:28+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" .
}