@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP154592.RAKJ0UXUanP_DXR1DsbPCQcUVguh-TLfw6TWhdeeoL-hY> .
@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:NP154592.RAKJ0UXUanP_DXR1DsbPCQcUVguh-TLfw6TWhdeeoL-hY130_head {
  this: np:hasAssertion dgn-np:NP154592.RAKJ0UXUanP_DXR1DsbPCQcUVguh-TLfw6TWhdeeoL-hY130_assertion;
    np:hasProvenance dgn-np:NP154592.RAKJ0UXUanP_DXR1DsbPCQcUVguh-TLfw6TWhdeeoL-hY130_provenance;
    np:hasPublicationInfo dgn-np:NP154592.RAKJ0UXUanP_DXR1DsbPCQcUVguh-TLfw6TWhdeeoL-hY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP154592.RAKJ0UXUanP_DXR1DsbPCQcUVguh-TLfw6TWhdeeoL-hY130_assertion a np:Assertion .
  
  dgn-np:NP154592.RAKJ0UXUanP_DXR1DsbPCQcUVguh-TLfw6TWhdeeoL-hY130_provenance a np:Provenance .
  
  dgn-np:NP154592.RAKJ0UXUanP_DXR1DsbPCQcUVguh-TLfw6TWhdeeoL-hY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP154592.RAKJ0UXUanP_DXR1DsbPCQcUVguh-TLfw6TWhdeeoL-hY130_assertion {
  miriam-gene:1536 a ncit:C16612 .
  
  lld:C1844376 a ncit:C7057 .
  
  dgn-gda:DGN10d3b6817ebd4af8e2ad36dea4ef8803 sio:SIO_000628 miriam-gene:1536, lld:C1844376;
    a sio:SIO_001121 .
}

dgn-np:NP154592.RAKJ0UXUanP_DXR1DsbPCQcUVguh-TLfw6TWhdeeoL-hY130_provenance {
  dgn-np:NP154592.RAKJ0UXUanP_DXR1DsbPCQcUVguh-TLfw6TWhdeeoL-hY130_assertion dcterms:description
      "[4) In PMA-stimulated B cells from an X91+ CGD patient in which p22phox was normally expressed and gp91phox was present but lacked five amino acids, translocation of p47phox to the membranes was unaffected, but p67phox and p40phox were poorly translocated, and the production of O2- was greatly reduced with respect to that by normal B 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:9794433;
    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:NP154592.RAKJ0UXUanP_DXR1DsbPCQcUVguh-TLfw6TWhdeeoL-hY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:22+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" .
}