@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP564301.RA7nudivQsGX7QCMp8ld6dY3OoMgae8KPbSqm8JSqhrfQ> .
@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:NP564301.RA7nudivQsGX7QCMp8ld6dY3OoMgae8KPbSqm8JSqhrfQ130_head {
  this: np:hasAssertion dgn-np:NP564301.RA7nudivQsGX7QCMp8ld6dY3OoMgae8KPbSqm8JSqhrfQ130_assertion ;
    np:hasProvenance dgn-np:NP564301.RA7nudivQsGX7QCMp8ld6dY3OoMgae8KPbSqm8JSqhrfQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP564301.RA7nudivQsGX7QCMp8ld6dY3OoMgae8KPbSqm8JSqhrfQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP564301.RA7nudivQsGX7QCMp8ld6dY3OoMgae8KPbSqm8JSqhrfQ130_assertion a np:Assertion .
  dgn-np:NP564301.RA7nudivQsGX7QCMp8ld6dY3OoMgae8KPbSqm8JSqhrfQ130_provenance a np:Provenance .
  dgn-np:NP564301.RA7nudivQsGX7QCMp8ld6dY3OoMgae8KPbSqm8JSqhrfQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP564301.RA7nudivQsGX7QCMp8ld6dY3OoMgae8KPbSqm8JSqhrfQ130_assertion {
  miriam-gene:2821 a ncit:C16612 .
  lld:C0031106 a ncit:C7057 .
  dgn-gda:DGNc721ae7bfedad265ab3f67abd62950f1 sio:SIO_000628 miriam-gene:2821 , lld:C0031106 ;
    a sio:SIO_001121 .
}
dgn-np:NP564301.RA7nudivQsGX7QCMp8ld6dY3OoMgae8KPbSqm8JSqhrfQ130_provenance {
  dgn-np:NP564301.RA7nudivQsGX7QCMp8ld6dY3OoMgae8KPbSqm8JSqhrfQ130_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:NP564301.RA7nudivQsGX7QCMp8ld6dY3OoMgae8KPbSqm8JSqhrfQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:40+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" .
}