@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP60333.RA3cQd3sBN7MlT2YiOg-o8i9cqpMQsupn3VhtU-X1oFII> .
@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 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:NP60333.RA3cQd3sBN7MlT2YiOg-o8i9cqpMQsupn3VhtU-X1oFII130_head {
  this: np:hasAssertion dgn-np:NP60333.RA3cQd3sBN7MlT2YiOg-o8i9cqpMQsupn3VhtU-X1oFII130_assertion;
    np:hasProvenance dgn-np:NP60333.RA3cQd3sBN7MlT2YiOg-o8i9cqpMQsupn3VhtU-X1oFII130_provenance;
    np:hasPublicationInfo dgn-np:NP60333.RA3cQd3sBN7MlT2YiOg-o8i9cqpMQsupn3VhtU-X1oFII130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP60333.RA3cQd3sBN7MlT2YiOg-o8i9cqpMQsupn3VhtU-X1oFII130_assertion a np:Assertion .
  
  dgn-np:NP60333.RA3cQd3sBN7MlT2YiOg-o8i9cqpMQsupn3VhtU-X1oFII130_provenance a np:Provenance .
  
  dgn-np:NP60333.RA3cQd3sBN7MlT2YiOg-o8i9cqpMQsupn3VhtU-X1oFII130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP60333.RA3cQd3sBN7MlT2YiOg-o8i9cqpMQsupn3VhtU-X1oFII130_assertion {
  miriam-gene:2215 a ncit:C16612 .
  
  lld:C0003873 a ncit:C7057 .
  
  dgn-gda:DGNd75ad2442daf555e699c90c13bb7ff16 sio:SIO_000628 miriam-gene:2215, lld:C0003873;
    a sio:SIO_001122 .
}

dgn-np:NP60333.RA3cQd3sBN7MlT2YiOg-o8i9cqpMQsupn3VhtU-X1oFII130_provenance {
  dgn-np:NP60333.RA3cQd3sBN7MlT2YiOg-o8i9cqpMQsupn3VhtU-X1oFII130_assertion dct:description
      "[The variant haplotype FCGR3B*1 A227G, which occurred in homozygosis in two Amerindians and in heterozygosis in two Afro-Brazilians, is described for the first time in the present report. In general, these data reveal variability in the frequency of alleles of the FCGR3B gene compared to other populations of the same genetic background in other regions of the world.]. 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:15713217;
    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:NP60333.RA3cQd3sBN7MlT2YiOg-o8i9cqpMQsupn3VhtU-X1oFII130_publicationInfo {
  this: dct:created "2014-10-02T12:32:28+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}