@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP438678.RASKUmLTxF5KNyIBsm0TJImdaopNQY__v41a3TbPswzAs> .
@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:NP438678.RASKUmLTxF5KNyIBsm0TJImdaopNQY__v41a3TbPswzAs130_head {
  this: np:hasAssertion dgn-np:NP438678.RASKUmLTxF5KNyIBsm0TJImdaopNQY__v41a3TbPswzAs130_assertion;
    np:hasProvenance dgn-np:NP438678.RASKUmLTxF5KNyIBsm0TJImdaopNQY__v41a3TbPswzAs130_provenance;
    np:hasPublicationInfo dgn-np:NP438678.RASKUmLTxF5KNyIBsm0TJImdaopNQY__v41a3TbPswzAs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP438678.RASKUmLTxF5KNyIBsm0TJImdaopNQY__v41a3TbPswzAs130_assertion a np:Assertion .
  
  dgn-np:NP438678.RASKUmLTxF5KNyIBsm0TJImdaopNQY__v41a3TbPswzAs130_provenance a np:Provenance .
  
  dgn-np:NP438678.RASKUmLTxF5KNyIBsm0TJImdaopNQY__v41a3TbPswzAs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP438678.RASKUmLTxF5KNyIBsm0TJImdaopNQY__v41a3TbPswzAs130_assertion {
  miriam-gene:4519 a ncit:C16612 .
  
  lld:C0018203 a ncit:C7057 .
  
  dgn-gda:DGN01940752e1d7462c96db1a69e5e19884 sio:SIO_000628 miriam-gene:4519, lld:C0018203;
    a sio:SIO_001121 .
}

dgn-np:NP438678.RASKUmLTxF5KNyIBsm0TJImdaopNQY__v41a3TbPswzAs130_provenance {
  dgn-np:NP438678.RASKUmLTxF5KNyIBsm0TJImdaopNQY__v41a3TbPswzAs130_assertion dcterms:description
      "[The diagnosis of CGD in both the latest male patient and the index male was confirmed by marked impairment in polymorphonuclear leucocyte oxidative burst activity in association with absence of both subunits of cytochrome b.]. 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:10844491;
    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:NP438678.RASKUmLTxF5KNyIBsm0TJImdaopNQY__v41a3TbPswzAs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:19+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" .
}