@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP390253.RA4MIzIkubfM_5_ZGIu269otORDMs_ZXsaUB4eB9MjqQw> .
@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:NP390253.RA4MIzIkubfM_5_ZGIu269otORDMs_ZXsaUB4eB9MjqQw130_head {
  this: np:hasAssertion dgn-np:NP390253.RA4MIzIkubfM_5_ZGIu269otORDMs_ZXsaUB4eB9MjqQw130_assertion;
    np:hasProvenance dgn-np:NP390253.RA4MIzIkubfM_5_ZGIu269otORDMs_ZXsaUB4eB9MjqQw130_provenance;
    np:hasPublicationInfo dgn-np:NP390253.RA4MIzIkubfM_5_ZGIu269otORDMs_ZXsaUB4eB9MjqQw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP390253.RA4MIzIkubfM_5_ZGIu269otORDMs_ZXsaUB4eB9MjqQw130_assertion a np:Assertion .
  
  dgn-np:NP390253.RA4MIzIkubfM_5_ZGIu269otORDMs_ZXsaUB4eB9MjqQw130_provenance a np:Provenance .
  
  dgn-np:NP390253.RA4MIzIkubfM_5_ZGIu269otORDMs_ZXsaUB4eB9MjqQw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP390253.RA4MIzIkubfM_5_ZGIu269otORDMs_ZXsaUB4eB9MjqQw130_assertion {
  miriam-gene:2056 a ncit:C16612 .
  
  lld:C1851490 a ncit:C7057 .
  
  dgn-gda:DGN699392afee573f6c9db54a6a8399e26f sio:SIO_000628 miriam-gene:2056, lld:C1851490;
    a sio:SIO_001121 .
}

dgn-np:NP390253.RA4MIzIkubfM_5_ZGIu269otORDMs_ZXsaUB4eB9MjqQw130_provenance {
  dgn-np:NP390253.RA4MIzIkubfM_5_ZGIu269otORDMs_ZXsaUB4eB9MjqQw130_assertion dcterms:description
      "[Further in vitro analysis of the erythroid progenitor cells of this affected child revealed that the progenitor cells were hypersensitive to EPO (a hallmark of PFCP) suggesting the presence of the disease at the level of progenitor cells.]. 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:9649565;
    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:NP390253.RA4MIzIkubfM_5_ZGIu269otORDMs_ZXsaUB4eB9MjqQw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:52+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" .
}