@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP184629.RAUCZUCDYqOpUpCmDwUeY2cCH4WmC37mQmJM592AdvIy8> .
@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:NP184629.RAUCZUCDYqOpUpCmDwUeY2cCH4WmC37mQmJM592AdvIy8130_head {
  this: np:hasAssertion dgn-np:NP184629.RAUCZUCDYqOpUpCmDwUeY2cCH4WmC37mQmJM592AdvIy8130_assertion;
    np:hasProvenance dgn-np:NP184629.RAUCZUCDYqOpUpCmDwUeY2cCH4WmC37mQmJM592AdvIy8130_provenance;
    np:hasPublicationInfo dgn-np:NP184629.RAUCZUCDYqOpUpCmDwUeY2cCH4WmC37mQmJM592AdvIy8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP184629.RAUCZUCDYqOpUpCmDwUeY2cCH4WmC37mQmJM592AdvIy8130_assertion a np:Assertion .
  
  dgn-np:NP184629.RAUCZUCDYqOpUpCmDwUeY2cCH4WmC37mQmJM592AdvIy8130_provenance a np:Provenance .
  
  dgn-np:NP184629.RAUCZUCDYqOpUpCmDwUeY2cCH4WmC37mQmJM592AdvIy8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP184629.RAUCZUCDYqOpUpCmDwUeY2cCH4WmC37mQmJM592AdvIy8130_assertion {
  miriam-gene:1589 a ncit:C16612 .
  
  lld:C0004364 a ncit:C7057 .
  
  dgn-gda:DGNeb8f98c4c055c0b8ebe3da62f47c9e4f sio:SIO_000628 miriam-gene:1589, lld:C0004364;
    a sio:SIO_001121 .
}

dgn-np:NP184629.RAUCZUCDYqOpUpCmDwUeY2cCH4WmC37mQmJM592AdvIy8130_provenance {
  dgn-np:NP184629.RAUCZUCDYqOpUpCmDwUeY2cCH4WmC37mQmJM592AdvIy8130_assertion dcterms:description
      "[Several autoimmune disorders as well as congenital adrenal hyperplasia (CAH) are either associated or closely linked with genetic variants of the fourth component of complement (C4A and C4B) and the enzyme steroid 21-hydroxylase (21-OH).]. 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:3018042;
    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:NP184629.RAUCZUCDYqOpUpCmDwUeY2cCH4WmC37mQmJM592AdvIy8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:40+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" .
}