@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP451628.RAQNK47Bd_9Z0p164GR_KjkXgIN509rj_7J-weyzFP65U> .
@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:NP451628.RAQNK47Bd_9Z0p164GR_KjkXgIN509rj_7J-weyzFP65U130_head {
  this: np:hasAssertion dgn-np:NP451628.RAQNK47Bd_9Z0p164GR_KjkXgIN509rj_7J-weyzFP65U130_assertion;
    np:hasProvenance dgn-np:NP451628.RAQNK47Bd_9Z0p164GR_KjkXgIN509rj_7J-weyzFP65U130_provenance;
    np:hasPublicationInfo dgn-np:NP451628.RAQNK47Bd_9Z0p164GR_KjkXgIN509rj_7J-weyzFP65U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP451628.RAQNK47Bd_9Z0p164GR_KjkXgIN509rj_7J-weyzFP65U130_assertion a np:Assertion .
  
  dgn-np:NP451628.RAQNK47Bd_9Z0p164GR_KjkXgIN509rj_7J-weyzFP65U130_provenance a np:Provenance .
  
  dgn-np:NP451628.RAQNK47Bd_9Z0p164GR_KjkXgIN509rj_7J-weyzFP65U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP451628.RAQNK47Bd_9Z0p164GR_KjkXgIN509rj_7J-weyzFP65U130_assertion {
  miriam-gene:966 a ncit:C16612 .
  
  lld:C2676767 a ncit:C7057 .
  
  dgn-gda:DGN32e8af242622ba202f5017c5af5f35d3 sio:SIO_000628 miriam-gene:966, lld:C2676767;
    a sio:SIO_001121 .
}

dgn-np:NP451628.RAQNK47Bd_9Z0p164GR_KjkXgIN509rj_7J-weyzFP65U130_provenance {
  dgn-np:NP451628.RAQNK47Bd_9Z0p164GR_KjkXgIN509rj_7J-weyzFP65U130_assertion dcterms:description
      "[CD59 deficiency is a common finding in RBCs and WBCs in patients with chronic hemolysis suffering from paroxysmal nocturnal hemoglobinuria in which the acquired mutation in the PIGA gene leads to membrane loss of glycosylphosphatidylinositol-anchored membrane proteins, including CD59.]. 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:23149847;
    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:NP451628.RAQNK47Bd_9Z0p164GR_KjkXgIN509rj_7J-weyzFP65U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:29+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" .
}