@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP741777.RA1Y9OwhimI2OYTXU6zbhpUL812fyz1RykvarqdVT7Ghs> .
@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:NP741777.RA1Y9OwhimI2OYTXU6zbhpUL812fyz1RykvarqdVT7Ghs130_head {
  this: np:hasAssertion dgn-np:NP741777.RA1Y9OwhimI2OYTXU6zbhpUL812fyz1RykvarqdVT7Ghs130_assertion;
    np:hasProvenance dgn-np:NP741777.RA1Y9OwhimI2OYTXU6zbhpUL812fyz1RykvarqdVT7Ghs130_provenance;
    np:hasPublicationInfo dgn-np:NP741777.RA1Y9OwhimI2OYTXU6zbhpUL812fyz1RykvarqdVT7Ghs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP741777.RA1Y9OwhimI2OYTXU6zbhpUL812fyz1RykvarqdVT7Ghs130_assertion a np:Assertion .
  
  dgn-np:NP741777.RA1Y9OwhimI2OYTXU6zbhpUL812fyz1RykvarqdVT7Ghs130_provenance a np:Provenance .
  
  dgn-np:NP741777.RA1Y9OwhimI2OYTXU6zbhpUL812fyz1RykvarqdVT7Ghs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP741777.RA1Y9OwhimI2OYTXU6zbhpUL812fyz1RykvarqdVT7Ghs130_assertion {
  miriam-gene:101060521 a ncit:C16612 .
  
  lld:C0018203 a ncit:C7057 .
  
  dgn-gda:DGNeb858a4c0b632a82b52082b342a1ea5a sio:SIO_000628 miriam-gene:101060521,
      lld:C0018203;
    a sio:SIO_001121 .
}

dgn-np:NP741777.RA1Y9OwhimI2OYTXU6zbhpUL812fyz1RykvarqdVT7Ghs130_provenance {
  dgn-np:NP741777.RA1Y9OwhimI2OYTXU6zbhpUL812fyz1RykvarqdVT7Ghs130_assertion dcterms:description
      "[These results indicate that the miR223 promoter as an internal promoter within SIN gene therapy vectors is able to efficiently correct the CGD phenotype with negligible activity in hematopoietic progenitors, thereby limiting the risk of insertional oncogenesis and development of clonal dominance.]. 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:23489116;
    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:NP741777.RA1Y9OwhimI2OYTXU6zbhpUL812fyz1RykvarqdVT7Ghs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:30+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" .
}