@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP569298.RAhvCHbrdxUlUG4RMPg63FIV58dnRBOW63F9ug-ndOcT0> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP569298.RAhvCHbrdxUlUG4RMPg63FIV58dnRBOW63F9ug-ndOcT0130_head {
  this: np:hasAssertion dgn-np:NP569298.RAhvCHbrdxUlUG4RMPg63FIV58dnRBOW63F9ug-ndOcT0130_assertion;
    np:hasProvenance dgn-np:NP569298.RAhvCHbrdxUlUG4RMPg63FIV58dnRBOW63F9ug-ndOcT0130_provenance;
    np:hasPublicationInfo dgn-np:NP569298.RAhvCHbrdxUlUG4RMPg63FIV58dnRBOW63F9ug-ndOcT0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP569298.RAhvCHbrdxUlUG4RMPg63FIV58dnRBOW63F9ug-ndOcT0130_assertion a np:Assertion .
  
  dgn-np:NP569298.RAhvCHbrdxUlUG4RMPg63FIV58dnRBOW63F9ug-ndOcT0130_provenance a np:Provenance .
  
  dgn-np:NP569298.RAhvCHbrdxUlUG4RMPg63FIV58dnRBOW63F9ug-ndOcT0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP569298.RAhvCHbrdxUlUG4RMPg63FIV58dnRBOW63F9ug-ndOcT0130_assertion {
  miriam-gene:653361 a ncit:C16612 .
  
  lld:C0018203 a ncit:C7057 .
  
  dgn-gda:DGNc2dc255c9ce44c68fdcf8fb5b3b71598 sio:SIO_000628 miriam-gene:653361, lld:C0018203;
    a sio:SIO_001121 .
}

dgn-np:NP569298.RAhvCHbrdxUlUG4RMPg63FIV58dnRBOW63F9ug-ndOcT0130_provenance {
  dgn-np:NP569298.RAhvCHbrdxUlUG4RMPg63FIV58dnRBOW63F9ug-ndOcT0130_assertion dcterms:description
      "[With this method we now found, in three CGD families patients with the normal number of two intact NCF1 genes (and four psiNCF1 genes) and in six CGD families, patients with one intact NCF1 gene (and five psiNCF1 genes).]. 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:16972229;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP569298.RAhvCHbrdxUlUG4RMPg63FIV58dnRBOW63F9ug-ndOcT0130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:03+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}