@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP346291.RAAGa4KjaenOvoT7CMI7vh8RiB5gZS2WlkugOLfAI-W64> .
@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:NP346291.RAAGa4KjaenOvoT7CMI7vh8RiB5gZS2WlkugOLfAI-W64130_head {
  this: np:hasAssertion dgn-np:NP346291.RAAGa4KjaenOvoT7CMI7vh8RiB5gZS2WlkugOLfAI-W64130_assertion;
    np:hasProvenance dgn-np:NP346291.RAAGa4KjaenOvoT7CMI7vh8RiB5gZS2WlkugOLfAI-W64130_provenance;
    np:hasPublicationInfo dgn-np:NP346291.RAAGa4KjaenOvoT7CMI7vh8RiB5gZS2WlkugOLfAI-W64130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP346291.RAAGa4KjaenOvoT7CMI7vh8RiB5gZS2WlkugOLfAI-W64130_assertion a np:Assertion .
  
  dgn-np:NP346291.RAAGa4KjaenOvoT7CMI7vh8RiB5gZS2WlkugOLfAI-W64130_provenance a np:Provenance .
  
  dgn-np:NP346291.RAAGa4KjaenOvoT7CMI7vh8RiB5gZS2WlkugOLfAI-W64130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP346291.RAAGa4KjaenOvoT7CMI7vh8RiB5gZS2WlkugOLfAI-W64130_assertion {
  miriam-gene:1236 a ncit:C16612 .
  
  lld:C0002871 a ncit:C7057 .
  
  dgn-gda:DGN9d0d9f08a802f95d5960946e08d21eb2 sio:SIO_000628 miriam-gene:1236, lld:C0002871;
    a sio:SIO_001121 .
}

dgn-np:NP346291.RAAGa4KjaenOvoT7CMI7vh8RiB5gZS2WlkugOLfAI-W64130_provenance {
  dgn-np:NP346291.RAAGa4KjaenOvoT7CMI7vh8RiB5gZS2WlkugOLfAI-W64130_assertion dcterms:description
      "[We earlier reported on a mouse model that constitutive expression of EVI1 in the BM led to fatal anemia and myeloid dysplasia, as observed in MDS patients, and we subsequently showed that EVI1 interaction with GATA1 blocks proper erythropoiesis.]. 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:19208846;
    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:NP346291.RAAGa4KjaenOvoT7CMI7vh8RiB5gZS2WlkugOLfAI-W64130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:23+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" .
}