@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP532597.RAFkQw7iDsI7mKjv8vBaAnIPIXCnNnnaOXq_MinS06oGg> .
@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:NP532597.RAFkQw7iDsI7mKjv8vBaAnIPIXCnNnnaOXq_MinS06oGg130_head {
  this: np:hasAssertion dgn-np:NP532597.RAFkQw7iDsI7mKjv8vBaAnIPIXCnNnnaOXq_MinS06oGg130_assertion;
    np:hasProvenance dgn-np:NP532597.RAFkQw7iDsI7mKjv8vBaAnIPIXCnNnnaOXq_MinS06oGg130_provenance;
    np:hasPublicationInfo dgn-np:NP532597.RAFkQw7iDsI7mKjv8vBaAnIPIXCnNnnaOXq_MinS06oGg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP532597.RAFkQw7iDsI7mKjv8vBaAnIPIXCnNnnaOXq_MinS06oGg130_assertion a np:Assertion .
  
  dgn-np:NP532597.RAFkQw7iDsI7mKjv8vBaAnIPIXCnNnnaOXq_MinS06oGg130_provenance a np:Provenance .
  
  dgn-np:NP532597.RAFkQw7iDsI7mKjv8vBaAnIPIXCnNnnaOXq_MinS06oGg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP532597.RAFkQw7iDsI7mKjv8vBaAnIPIXCnNnnaOXq_MinS06oGg130_assertion {
  miriam-gene:720 a ncit:C16612 .
  
  lld:C0004364 a ncit:C7057 .
  
  dgn-gda:DGN6527d5e30b7c049033f29770f7905e4b sio:SIO_000628 miriam-gene:720, lld:C0004364;
    a sio:SIO_001121 .
}

dgn-np:NP532597.RAFkQw7iDsI7mKjv8vBaAnIPIXCnNnnaOXq_MinS06oGg130_provenance {
  dgn-np:NP532597.RAFkQw7iDsI7mKjv8vBaAnIPIXCnNnnaOXq_MinS06oGg130_assertion dcterms:description
      "[Interindividual gene copy-number variation (CNV) of complement component C4 and its associated polymorphisms in gene size (long and short) and protein isotypes (C4A and C4B) probably lead to different susceptibilities to autoimmune disease.]. 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:17503323;
    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:NP532597.RAFkQw7iDsI7mKjv8vBaAnIPIXCnNnnaOXq_MinS06oGg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:21+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" .
}