@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP60318.RAipHzxGYdQ_wrA1cOrIO-cqgzKs5qg1ypcvqRJYBZUSs> .
@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:NP60318.RAipHzxGYdQ_wrA1cOrIO-cqgzKs5qg1ypcvqRJYBZUSs130_head {
  this: np:hasAssertion dgn-np:NP60318.RAipHzxGYdQ_wrA1cOrIO-cqgzKs5qg1ypcvqRJYBZUSs130_assertion;
    np:hasProvenance dgn-np:NP60318.RAipHzxGYdQ_wrA1cOrIO-cqgzKs5qg1ypcvqRJYBZUSs130_provenance;
    np:hasPublicationInfo dgn-np:NP60318.RAipHzxGYdQ_wrA1cOrIO-cqgzKs5qg1ypcvqRJYBZUSs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP60318.RAipHzxGYdQ_wrA1cOrIO-cqgzKs5qg1ypcvqRJYBZUSs130_assertion a np:Assertion .
  
  dgn-np:NP60318.RAipHzxGYdQ_wrA1cOrIO-cqgzKs5qg1ypcvqRJYBZUSs130_provenance a np:Provenance .
  
  dgn-np:NP60318.RAipHzxGYdQ_wrA1cOrIO-cqgzKs5qg1ypcvqRJYBZUSs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP60318.RAipHzxGYdQ_wrA1cOrIO-cqgzKs5qg1ypcvqRJYBZUSs130_assertion {
  miriam-gene:2215 a ncit:C16612 .
  
  lld:C0031090 a ncit:C7057 .
  
  dgn-gda:DGN876072f33d13897b04e93b4b0a2d7d99 sio:SIO_000628 miriam-gene:2215, lld:C0031090;
    a sio:SIO_001122 .
}

dgn-np:NP60318.RAipHzxGYdQ_wrA1cOrIO-cqgzKs5qg1ypcvqRJYBZUSs130_provenance {
  dgn-np:NP60318.RAipHzxGYdQ_wrA1cOrIO-cqgzKs5qg1ypcvqRJYBZUSs130_assertion dcterms:description
      "[ The coincidence of the three known FCGR3B alleles varies within the population of Germany and Uganda. Three simultaneous FCGR3B forms may be explained by two gene loci, but the basis of the high number of different variants in some individuals still remains unclear. Possible explanations may be a hypermutation mechanism or a number of FCGR3 higher than expected hitherto.]. 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:12076295;
    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:NP60318.RAipHzxGYdQ_wrA1cOrIO-cqgzKs5qg1ypcvqRJYBZUSs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:28+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" .
}