@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP872925.RAc20-q6DwqMzN8lcBsMfT-3dnVZWyd34HDm1UgyDUPfI> .
@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:NP872925.RAc20-q6DwqMzN8lcBsMfT-3dnVZWyd34HDm1UgyDUPfI130_head {
  this: np:hasAssertion dgn-np:NP872925.RAc20-q6DwqMzN8lcBsMfT-3dnVZWyd34HDm1UgyDUPfI130_assertion;
    np:hasProvenance dgn-np:NP872925.RAc20-q6DwqMzN8lcBsMfT-3dnVZWyd34HDm1UgyDUPfI130_provenance;
    np:hasPublicationInfo dgn-np:NP872925.RAc20-q6DwqMzN8lcBsMfT-3dnVZWyd34HDm1UgyDUPfI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP872925.RAc20-q6DwqMzN8lcBsMfT-3dnVZWyd34HDm1UgyDUPfI130_assertion a np:Assertion .
  
  dgn-np:NP872925.RAc20-q6DwqMzN8lcBsMfT-3dnVZWyd34HDm1UgyDUPfI130_provenance a np:Provenance .
  
  dgn-np:NP872925.RAc20-q6DwqMzN8lcBsMfT-3dnVZWyd34HDm1UgyDUPfI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP872925.RAc20-q6DwqMzN8lcBsMfT-3dnVZWyd34HDm1UgyDUPfI130_assertion {
  miriam-gene:728 a ncit:C16612 .
  
  lld:C0004096 a ncit:C7057 .
  
  dgn-gda:DGN7ae52704db7d1699656b143b3057b9a0 sio:SIO_000628 miriam-gene:728, lld:C0004096;
    a sio:SIO_001121 .
}

dgn-np:NP872925.RAc20-q6DwqMzN8lcBsMfT-3dnVZWyd34HDm1UgyDUPfI130_provenance {
  dgn-np:NP872925.RAc20-q6DwqMzN8lcBsMfT-3dnVZWyd34HDm1UgyDUPfI130_assertion dcterms:description
      "[To determine whether genetic variations in the genes of the complement system affect susceptibility to BA, we screened single nucleotide polymorphisms (SNPs) in C3, C5, the C3a receptor gene (C3AR1), and the C5a receptor gene (C5R1) and performed association studies in the Japanese population.]. 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: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:NP872925.RAc20-q6DwqMzN8lcBsMfT-3dnVZWyd34HDm1UgyDUPfI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:53+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" .
}