@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP673332.RArvXwyFpRvOk4Z8GycH1BbuyujKacWVZYIlYiQsGlB58> .
@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:NP673332.RArvXwyFpRvOk4Z8GycH1BbuyujKacWVZYIlYiQsGlB58130_head {
  this: np:hasAssertion dgn-np:NP673332.RArvXwyFpRvOk4Z8GycH1BbuyujKacWVZYIlYiQsGlB58130_assertion ;
    np:hasProvenance dgn-np:NP673332.RArvXwyFpRvOk4Z8GycH1BbuyujKacWVZYIlYiQsGlB58130_provenance ;
    np:hasPublicationInfo dgn-np:NP673332.RArvXwyFpRvOk4Z8GycH1BbuyujKacWVZYIlYiQsGlB58130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP673332.RArvXwyFpRvOk4Z8GycH1BbuyujKacWVZYIlYiQsGlB58130_assertion a np:Assertion .
  dgn-np:NP673332.RArvXwyFpRvOk4Z8GycH1BbuyujKacWVZYIlYiQsGlB58130_provenance a np:Provenance .
  dgn-np:NP673332.RArvXwyFpRvOk4Z8GycH1BbuyujKacWVZYIlYiQsGlB58130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP673332.RArvXwyFpRvOk4Z8GycH1BbuyujKacWVZYIlYiQsGlB58130_assertion {
  miriam-gene:4082 a ncit:C16612 .
  lld:C0001815 a ncit:C7057 .
  dgn-gda:DGNebab7a5f5b367100fdc90ea6cd671b96 sio:SIO_000628 miriam-gene:4082 , lld:C0001815 ;
    a sio:SIO_001121 .
}
dgn-np:NP673332.RArvXwyFpRvOk4Z8GycH1BbuyujKacWVZYIlYiQsGlB58130_provenance {
  dgn-np:NP673332.RArvXwyFpRvOk4Z8GycH1BbuyujKacWVZYIlYiQsGlB58130_assertion dcterms:description "[A combination of magnetic cell sorting (MACS) and fluorescent in situ hybridization (FISH) techniques was used to detect clonal cytogenetic markers in different myeloid and lymphoid cell types of the peripheral blood from 4 patients with myelofibrosis with myeloid metaplasia (MMM) that was associated with either a 13q- or a 20q- karyotypic abnormality.]. 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:12406879 ;
    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:NP673332.RArvXwyFpRvOk4Z8GycH1BbuyujKacWVZYIlYiQsGlB58130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:46+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" .
}