@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP63134.RAWeWf3iknNwSn_yQFaRWNUJqG-e78lC1ZMZWbdxKLXLg> .
@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:NP63134.RAWeWf3iknNwSn_yQFaRWNUJqG-e78lC1ZMZWbdxKLXLg130_head {
  this: np:hasAssertion dgn-np:NP63134.RAWeWf3iknNwSn_yQFaRWNUJqG-e78lC1ZMZWbdxKLXLg130_assertion;
    np:hasProvenance dgn-np:NP63134.RAWeWf3iknNwSn_yQFaRWNUJqG-e78lC1ZMZWbdxKLXLg130_provenance;
    np:hasPublicationInfo dgn-np:NP63134.RAWeWf3iknNwSn_yQFaRWNUJqG-e78lC1ZMZWbdxKLXLg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP63134.RAWeWf3iknNwSn_yQFaRWNUJqG-e78lC1ZMZWbdxKLXLg130_assertion a np:Assertion .
  
  dgn-np:NP63134.RAWeWf3iknNwSn_yQFaRWNUJqG-e78lC1ZMZWbdxKLXLg130_provenance a np:Provenance .
  
  dgn-np:NP63134.RAWeWf3iknNwSn_yQFaRWNUJqG-e78lC1ZMZWbdxKLXLg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP63134.RAWeWf3iknNwSn_yQFaRWNUJqG-e78lC1ZMZWbdxKLXLg130_assertion {
  miriam-gene:728 a ncit:C16612 .
  
  lld:C0004096 a ncit:C7057 .
  
  dgn-gda:DGN7fd348722c348506d31f67660f56ca9c sio:SIO_000628 miriam-gene:728, lld:C0004096;
    a sio:SIO_001122 .
}

dgn-np:NP63134.RAWeWf3iknNwSn_yQFaRWNUJqG-e78lC1ZMZWbdxKLXLg130_provenance {
  dgn-np:NP63134.RAWeWf3iknNwSn_yQFaRWNUJqG-e78lC1ZMZWbdxKLXLg130_assertion dcterms:description
      "[These results suggest that the C3 and C5 pathways of the complement system play important roles in the pathogenesis of BA and that polymorphisms of these genes affect susceptibility to BA.]. 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:15278436;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP63134.RAWeWf3iknNwSn_yQFaRWNUJqG-e78lC1ZMZWbdxKLXLg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:30+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;
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}