@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP726804.RAiUjA8cl5WqzDKvRjIEkwu0XOOeeqpu5EbR7Ot_mvFck> .
@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:NP726804.RAiUjA8cl5WqzDKvRjIEkwu0XOOeeqpu5EbR7Ot_mvFck130_head {
  this: np:hasAssertion dgn-np:NP726804.RAiUjA8cl5WqzDKvRjIEkwu0XOOeeqpu5EbR7Ot_mvFck130_assertion ;
    np:hasProvenance dgn-np:NP726804.RAiUjA8cl5WqzDKvRjIEkwu0XOOeeqpu5EbR7Ot_mvFck130_provenance ;
    np:hasPublicationInfo dgn-np:NP726804.RAiUjA8cl5WqzDKvRjIEkwu0XOOeeqpu5EbR7Ot_mvFck130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP726804.RAiUjA8cl5WqzDKvRjIEkwu0XOOeeqpu5EbR7Ot_mvFck130_assertion a np:Assertion .
  dgn-np:NP726804.RAiUjA8cl5WqzDKvRjIEkwu0XOOeeqpu5EbR7Ot_mvFck130_provenance a np:Provenance .
  dgn-np:NP726804.RAiUjA8cl5WqzDKvRjIEkwu0XOOeeqpu5EbR7Ot_mvFck130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP726804.RAiUjA8cl5WqzDKvRjIEkwu0XOOeeqpu5EbR7Ot_mvFck130_assertion {
  miriam-gene:54453 a ncit:C16612 .
  lld:C0001815 a ncit:C7057 .
  dgn-gda:DGNc1a9f93b87c048ab52cead0bdecb587d sio:SIO_000628 miriam-gene:54453 , lld:C0001815 ;
    a sio:SIO_001121 .
}
dgn-np:NP726804.RAiUjA8cl5WqzDKvRjIEkwu0XOOeeqpu5EbR7Ot_mvFck130_provenance {
  dgn-np:NP726804.RAiUjA8cl5WqzDKvRjIEkwu0XOOeeqpu5EbR7Ot_mvFck130_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:NP726804.RAiUjA8cl5WqzDKvRjIEkwu0XOOeeqpu5EbR7Ot_mvFck130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:21+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" .
}