@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP387737.RAclvkvn8M7f8Oq4VB7rSKW9TEiyt7dpWOiw_BxqmfozA> .
@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:NP387737.RAclvkvn8M7f8Oq4VB7rSKW9TEiyt7dpWOiw_BxqmfozA130_head {
  this: np:hasAssertion dgn-np:NP387737.RAclvkvn8M7f8Oq4VB7rSKW9TEiyt7dpWOiw_BxqmfozA130_assertion;
    np:hasProvenance dgn-np:NP387737.RAclvkvn8M7f8Oq4VB7rSKW9TEiyt7dpWOiw_BxqmfozA130_provenance;
    np:hasPublicationInfo dgn-np:NP387737.RAclvkvn8M7f8Oq4VB7rSKW9TEiyt7dpWOiw_BxqmfozA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP387737.RAclvkvn8M7f8Oq4VB7rSKW9TEiyt7dpWOiw_BxqmfozA130_assertion a np:Assertion .
  
  dgn-np:NP387737.RAclvkvn8M7f8Oq4VB7rSKW9TEiyt7dpWOiw_BxqmfozA130_provenance a np:Provenance .
  
  dgn-np:NP387737.RAclvkvn8M7f8Oq4VB7rSKW9TEiyt7dpWOiw_BxqmfozA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP387737.RAclvkvn8M7f8Oq4VB7rSKW9TEiyt7dpWOiw_BxqmfozA130_assertion {
  miriam-gene:10007 a ncit:C16612 .
  
  lld:C0399447 a ncit:C7057 .
  
  dgn-gda:DGNda3ef1d348671995fa7ea216f993b0a6 sio:SIO_000628 miriam-gene:10007, lld:C0399447;
    a sio:SIO_001121 .
}

dgn-np:NP387737.RAclvkvn8M7f8Oq4VB7rSKW9TEiyt7dpWOiw_BxqmfozA130_provenance {
  dgn-np:NP387737.RAclvkvn8M7f8Oq4VB7rSKW9TEiyt7dpWOiw_BxqmfozA130_assertion dcterms:description
      "[GPI anchors of CD16 on neutrophils from controls and patients were both partially resistant to phosphatidylinositol-specific phospholipase C. The presence of promyelocytes in peripheral blood, low expression of CD16, and low chemotactic response of neutrophils suggest that patients with EOP have an abnormal maturation system in myeloid lineage cells in the bone marrow, which may be associated with the onset and course of EOP.]. 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:9284170;
    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:NP387737.RAclvkvn8M7f8Oq4VB7rSKW9TEiyt7dpWOiw_BxqmfozA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:51+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" .
}