@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP852926.RAHmsDy1-o6771OvjoOV6-TGM6jqtZCG2XolB9NsKBZ_0> .
@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:NP852926.RAHmsDy1-o6771OvjoOV6-TGM6jqtZCG2XolB9NsKBZ_0130_head {
  this: np:hasAssertion dgn-np:NP852926.RAHmsDy1-o6771OvjoOV6-TGM6jqtZCG2XolB9NsKBZ_0130_assertion;
    np:hasProvenance dgn-np:NP852926.RAHmsDy1-o6771OvjoOV6-TGM6jqtZCG2XolB9NsKBZ_0130_provenance;
    np:hasPublicationInfo dgn-np:NP852926.RAHmsDy1-o6771OvjoOV6-TGM6jqtZCG2XolB9NsKBZ_0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP852926.RAHmsDy1-o6771OvjoOV6-TGM6jqtZCG2XolB9NsKBZ_0130_assertion a np:Assertion .
  
  dgn-np:NP852926.RAHmsDy1-o6771OvjoOV6-TGM6jqtZCG2XolB9NsKBZ_0130_provenance a np:Provenance .
  
  dgn-np:NP852926.RAHmsDy1-o6771OvjoOV6-TGM6jqtZCG2XolB9NsKBZ_0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP852926.RAHmsDy1-o6771OvjoOV6-TGM6jqtZCG2XolB9NsKBZ_0130_assertion {
  miriam-gene:8996 a ncit:C16612 .
  
  lld:C0026986 a ncit:C7057 .
  
  dgn-gda:DGNceb95e9052bfcae3956a848ff8441780 sio:SIO_000628 miriam-gene:8996, lld:C0026986;
    a sio:SIO_001121 .
}

dgn-np:NP852926.RAHmsDy1-o6771OvjoOV6-TGM6jqtZCG2XolB9NsKBZ_0130_provenance {
  dgn-np:NP852926.RAHmsDy1-o6771OvjoOV6-TGM6jqtZCG2XolB9NsKBZ_0130_assertion dcterms:description
      "[In 431 patients presenting with unexplained cytopenia(s) FCM results were compared to abnormal karyotyping and FISH results recognized as associated with myelodysplastic syndrome (MDS) in the 2008 WHO classification, to assess the degree of and types of phenotypic abnormalities observed using a previously reported flow cytometric scoring system (FCSS).]. 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:21520402;
    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:NP852926.RAHmsDy1-o6771OvjoOV6-TGM6jqtZCG2XolB9NsKBZ_0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:41+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" .
}