@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP803959.RAHfzsqMCjLglx0NsDwX_dyp3dy_uLcTQv7qSe47nkvs0> .
@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:NP803959.RAHfzsqMCjLglx0NsDwX_dyp3dy_uLcTQv7qSe47nkvs0130_head {
  this: np:hasAssertion dgn-np:NP803959.RAHfzsqMCjLglx0NsDwX_dyp3dy_uLcTQv7qSe47nkvs0130_assertion ;
    np:hasProvenance dgn-np:NP803959.RAHfzsqMCjLglx0NsDwX_dyp3dy_uLcTQv7qSe47nkvs0130_provenance ;
    np:hasPublicationInfo dgn-np:NP803959.RAHfzsqMCjLglx0NsDwX_dyp3dy_uLcTQv7qSe47nkvs0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP803959.RAHfzsqMCjLglx0NsDwX_dyp3dy_uLcTQv7qSe47nkvs0130_assertion a np:Assertion .
  dgn-np:NP803959.RAHfzsqMCjLglx0NsDwX_dyp3dy_uLcTQv7qSe47nkvs0130_provenance a np:Provenance .
  dgn-np:NP803959.RAHfzsqMCjLglx0NsDwX_dyp3dy_uLcTQv7qSe47nkvs0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP803959.RAHfzsqMCjLglx0NsDwX_dyp3dy_uLcTQv7qSe47nkvs0130_assertion {
  miriam-gene:3562 a ncit:C16612 .
  lld:C0026986 a ncit:C7057 .
  dgn-gda:DGNcfbadbaf5eea428918742a89b2d19af9 sio:SIO_000628 miriam-gene:3562 , lld:C0026986 ;
    a sio:SIO_001121 .
}
dgn-np:NP803959.RAHfzsqMCjLglx0NsDwX_dyp3dy_uLcTQv7qSe47nkvs0130_provenance {
  dgn-np:NP803959.RAHfzsqMCjLglx0NsDwX_dyp3dy_uLcTQv7qSe47nkvs0130_assertion dcterms:description "[Restriction fragment length polymorphisms (RFLP) of the X-chromosome genes phosphoglycerate kinase and hypoxanthine phosphoribosyl transferase were used in conjunction with cytogenetic analysis to study the clonality of hematopoiesis in four female patients with myelodysplastic syndromes, treated with either granulocyte-macrophage colony-stimulating factor (GM-CSF) or interleukin-3 (IL-3), and in one patient with essential thrombocythemia (ET) treated with IL-3.]. 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:1676079 ;
    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:NP803959.RAHfzsqMCjLglx0NsDwX_dyp3dy_uLcTQv7qSe47nkvs0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:13+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" .
}