@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP919587.RATD3KV4kAgsvSEeph3qOuZgLv45fgtLDX8iDAAbYNFz0> .
@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:NP919587.RATD3KV4kAgsvSEeph3qOuZgLv45fgtLDX8iDAAbYNFz0130_head {
   this: np:hasAssertion dgn-np:NP919587.RATD3KV4kAgsvSEeph3qOuZgLv45fgtLDX8iDAAbYNFz0130_assertion ;
    np:hasProvenance dgn-np:NP919587.RATD3KV4kAgsvSEeph3qOuZgLv45fgtLDX8iDAAbYNFz0130_provenance ;
    np:hasPublicationInfo dgn-np:NP919587.RATD3KV4kAgsvSEeph3qOuZgLv45fgtLDX8iDAAbYNFz0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP919587.RATD3KV4kAgsvSEeph3qOuZgLv45fgtLDX8iDAAbYNFz0130_assertion a np:Assertion .
  dgn-np:NP919587.RATD3KV4kAgsvSEeph3qOuZgLv45fgtLDX8iDAAbYNFz0130_provenance a np:Provenance .
  dgn-np:NP919587.RATD3KV4kAgsvSEeph3qOuZgLv45fgtLDX8iDAAbYNFz0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP919587.RATD3KV4kAgsvSEeph3qOuZgLv45fgtLDX8iDAAbYNFz0130_assertion {
   miriam-gene:2056 a ncit:C16612 .
  lld:C0002893 a ncit:C7057 .
  dgn-gda:DGNfbea7a925f7a270c2f56a3a4a0f25f4d sio:SIO_000628 miriam-gene:2056 , lld:C0002893 ;
    a sio:SIO_001121 .
}
dgn-np:NP919587.RATD3KV4kAgsvSEeph3qOuZgLv45fgtLDX8iDAAbYNFz0130_provenance {
   dgn-np:NP919587.RATD3KV4kAgsvSEeph3qOuZgLv45fgtLDX8iDAAbYNFz0130_assertion dcterms:description "[We report a case of hypoplastic myelodyplastic syndrome (MDS) (refractory anemia (RA)) in which sustained trilineage haematological response and persistent disappearance of an abnormal chromosome clone were achieved after treatment with combination therapy of cytokines (granulocyte colony-stimulating factor (G-CSF) and erythropoietin (Epo)) and methylprednisolone (mPSL) pulse dose.]. 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:8611449 ;
    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:NP919587.RATD3KV4kAgsvSEeph3qOuZgLv45fgtLDX8iDAAbYNFz0130_publicationInfo {
   this: dcterms:created "2014-10-02T12:41:24+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" .
}