@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP605816.RAMl_-PbSx1IVea9nmAGabriCMdZ5Y2YXX3W7sO_7s1BA> .
@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:NP605816.RAMl_-PbSx1IVea9nmAGabriCMdZ5Y2YXX3W7sO_7s1BA130_head {
  this: np:hasAssertion dgn-np:NP605816.RAMl_-PbSx1IVea9nmAGabriCMdZ5Y2YXX3W7sO_7s1BA130_assertion;
    np:hasProvenance dgn-np:NP605816.RAMl_-PbSx1IVea9nmAGabriCMdZ5Y2YXX3W7sO_7s1BA130_provenance;
    np:hasPublicationInfo dgn-np:NP605816.RAMl_-PbSx1IVea9nmAGabriCMdZ5Y2YXX3W7sO_7s1BA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP605816.RAMl_-PbSx1IVea9nmAGabriCMdZ5Y2YXX3W7sO_7s1BA130_assertion a np:Assertion .
  
  dgn-np:NP605816.RAMl_-PbSx1IVea9nmAGabriCMdZ5Y2YXX3W7sO_7s1BA130_provenance a np:Provenance .
  
  dgn-np:NP605816.RAMl_-PbSx1IVea9nmAGabriCMdZ5Y2YXX3W7sO_7s1BA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP605816.RAMl_-PbSx1IVea9nmAGabriCMdZ5Y2YXX3W7sO_7s1BA130_assertion {
  miriam-gene:4353 a ncit:C16612 .
  
  lld:C0398595 a ncit:C7057 .
  
  dgn-gda:DGN3be58117fddfb54029419578b77adacd sio:SIO_000628 miriam-gene:4353, lld:C0398595;
    a sio:SIO_001121 .
}

dgn-np:NP605816.RAMl_-PbSx1IVea9nmAGabriCMdZ5Y2YXX3W7sO_7s1BA130_provenance {
  dgn-np:NP605816.RAMl_-PbSx1IVea9nmAGabriCMdZ5Y2YXX3W7sO_7s1BA130_assertion dcterms:description
      "[Although the contribution of myeloperoxidase to the chemiluminescence assay has been noted, the possible diagnostic confusion between chronic granulomatous disease of childhood (which is rare and severe) and myeloperoxidase deficiency (which is common and of little clinical consequence) has not been stressed.]. 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:6297833;
    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:NP605816.RAMl_-PbSx1IVea9nmAGabriCMdZ5Y2YXX3W7sO_7s1BA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:03+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: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" .
}