@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP189709.RAZgyEzYCXjVa_7myJRQKN6TgrfpKoDx1A5II2bvRYv0Q> .
@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:NP189709.RAZgyEzYCXjVa_7myJRQKN6TgrfpKoDx1A5II2bvRYv0Q130_head {
  this: np:hasAssertion dgn-np:NP189709.RAZgyEzYCXjVa_7myJRQKN6TgrfpKoDx1A5II2bvRYv0Q130_assertion;
    np:hasProvenance dgn-np:NP189709.RAZgyEzYCXjVa_7myJRQKN6TgrfpKoDx1A5II2bvRYv0Q130_provenance;
    np:hasPublicationInfo dgn-np:NP189709.RAZgyEzYCXjVa_7myJRQKN6TgrfpKoDx1A5II2bvRYv0Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP189709.RAZgyEzYCXjVa_7myJRQKN6TgrfpKoDx1A5II2bvRYv0Q130_assertion a np:Assertion .
  
  dgn-np:NP189709.RAZgyEzYCXjVa_7myJRQKN6TgrfpKoDx1A5II2bvRYv0Q130_provenance a np:Provenance .
  
  dgn-np:NP189709.RAZgyEzYCXjVa_7myJRQKN6TgrfpKoDx1A5II2bvRYv0Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP189709.RAZgyEzYCXjVa_7myJRQKN6TgrfpKoDx1A5II2bvRYv0Q130_assertion {
  miriam-gene:2214 a ncit:C16612 .
  
  lld:C0022658 a ncit:C7057 .
  
  dgn-gda:DGN7b95b2e3fc59686216b75cf9f0234059 sio:SIO_000628 miriam-gene:2214, lld:C0022658;
    a sio:SIO_001121 .
}

dgn-np:NP189709.RAZgyEzYCXjVa_7myJRQKN6TgrfpKoDx1A5II2bvRYv0Q130_provenance {
  dgn-np:NP189709.RAZgyEzYCXjVa_7myJRQKN6TgrfpKoDx1A5II2bvRYv0Q130_assertion dcterms:description
      "[Since the frequency distribution of FCGR3A alleles does not vary significantly among the ethnic groups studied, the additional factors underlying the ethnic disparities in renal disease progression remain to be elucidated.]. 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:17076550;
    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:NP189709.RAZgyEzYCXjVa_7myJRQKN6TgrfpKoDx1A5II2bvRYv0Q130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:44+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" .
}