@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP607599.RAfV1JKH6ncVEmZFQMeflIp8SQHV_YsOYV_YXwV5SrGmU> .
@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:NP607599.RAfV1JKH6ncVEmZFQMeflIp8SQHV_YsOYV_YXwV5SrGmU130_head {
  this: np:hasAssertion dgn-np:NP607599.RAfV1JKH6ncVEmZFQMeflIp8SQHV_YsOYV_YXwV5SrGmU130_assertion;
    np:hasProvenance dgn-np:NP607599.RAfV1JKH6ncVEmZFQMeflIp8SQHV_YsOYV_YXwV5SrGmU130_provenance;
    np:hasPublicationInfo dgn-np:NP607599.RAfV1JKH6ncVEmZFQMeflIp8SQHV_YsOYV_YXwV5SrGmU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP607599.RAfV1JKH6ncVEmZFQMeflIp8SQHV_YsOYV_YXwV5SrGmU130_assertion a np:Assertion .
  
  dgn-np:NP607599.RAfV1JKH6ncVEmZFQMeflIp8SQHV_YsOYV_YXwV5SrGmU130_provenance a np:Provenance .
  
  dgn-np:NP607599.RAfV1JKH6ncVEmZFQMeflIp8SQHV_YsOYV_YXwV5SrGmU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP607599.RAfV1JKH6ncVEmZFQMeflIp8SQHV_YsOYV_YXwV5SrGmU130_assertion {
  miriam-gene:7356 a ncit:C16612 .
  
  lld:C0024141 a ncit:C7057 .
  
  dgn-gda:DGNbfcb68b76104d7cce20c533296224339 sio:SIO_000628 miriam-gene:7356, lld:C0024141;
    a sio:SIO_001121 .
}

dgn-np:NP607599.RAfV1JKH6ncVEmZFQMeflIp8SQHV_YsOYV_YXwV5SrGmU130_provenance {
  dgn-np:NP607599.RAfV1JKH6ncVEmZFQMeflIp8SQHV_YsOYV_YXwV5SrGmU130_assertion dcterms:description
      "[To detect the presence of polymorphisms in the UG coding sequence, the DNA of 109 patients with IgA nephropathy (IgAN), and 32 patients with systemic lupus erythematosus (SLE) were tested for the nucleotide sequence of all three UG exons by heteroduplex analysis.]. 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:12003994;
    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:NP607599.RAfV1JKH6ncVEmZFQMeflIp8SQHV_YsOYV_YXwV5SrGmU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:04+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" .
}