@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP301964.RAKvV2TRfWcaT8DYLGx4kpACScyoGoLhcDAVbSftuDLzE> .
@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:NP301964.RAKvV2TRfWcaT8DYLGx4kpACScyoGoLhcDAVbSftuDLzE130_head {
  this: np:hasAssertion dgn-np:NP301964.RAKvV2TRfWcaT8DYLGx4kpACScyoGoLhcDAVbSftuDLzE130_assertion ;
    np:hasProvenance dgn-np:NP301964.RAKvV2TRfWcaT8DYLGx4kpACScyoGoLhcDAVbSftuDLzE130_provenance ;
    np:hasPublicationInfo dgn-np:NP301964.RAKvV2TRfWcaT8DYLGx4kpACScyoGoLhcDAVbSftuDLzE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP301964.RAKvV2TRfWcaT8DYLGx4kpACScyoGoLhcDAVbSftuDLzE130_assertion a np:Assertion .
  dgn-np:NP301964.RAKvV2TRfWcaT8DYLGx4kpACScyoGoLhcDAVbSftuDLzE130_provenance a np:Provenance .
  dgn-np:NP301964.RAKvV2TRfWcaT8DYLGx4kpACScyoGoLhcDAVbSftuDLzE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP301964.RAKvV2TRfWcaT8DYLGx4kpACScyoGoLhcDAVbSftuDLzE130_assertion {
  miriam-gene:55907 a ncit:C16612 .
  lld:C0042384 a ncit:C7057 .
  dgn-gda:DGNa0c73a2969801eff8c706f4bbb4d474e sio:SIO_000628 miriam-gene:55907 , lld:C0042384 ;
    a sio:SIO_001121 .
}
dgn-np:NP301964.RAKvV2TRfWcaT8DYLGx4kpACScyoGoLhcDAVbSftuDLzE130_provenance {
  dgn-np:NP301964.RAKvV2TRfWcaT8DYLGx4kpACScyoGoLhcDAVbSftuDLzE130_assertion dcterms:description "[CSS has 2 major clinical subsets, antineutrophil cytoplasmic antibody (ANCA)-positive, with features of small-vessel vasculitis, and ANCA-negative, in which organ damage is mainly mediated by tissue eosinophilic infiltration; analysis of HLA-DRB4 in patients categorized by different numbers of vasculitic manifestations (purpura, alveolar hemorrhage, mononeuritis multiplex, rapidly progressive glomerulonephritis, and constitutional symptoms) showed that its frequency strongly correlated with the number of vasculitis symptoms (P for trend = 0.001).]. 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:17763415 ;
    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:NP301964.RAKvV2TRfWcaT8DYLGx4kpACScyoGoLhcDAVbSftuDLzE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:51+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" .
}