@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP548597.RAD-3bsh8jGkAIauE7QpkwmqbUuAkQUEdeA_aDrF9JD8s> .
@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:NP548597.RAD-3bsh8jGkAIauE7QpkwmqbUuAkQUEdeA_aDrF9JD8s130_head {
  this: np:hasAssertion dgn-np:NP548597.RAD-3bsh8jGkAIauE7QpkwmqbUuAkQUEdeA_aDrF9JD8s130_assertion;
    np:hasProvenance dgn-np:NP548597.RAD-3bsh8jGkAIauE7QpkwmqbUuAkQUEdeA_aDrF9JD8s130_provenance;
    np:hasPublicationInfo dgn-np:NP548597.RAD-3bsh8jGkAIauE7QpkwmqbUuAkQUEdeA_aDrF9JD8s130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP548597.RAD-3bsh8jGkAIauE7QpkwmqbUuAkQUEdeA_aDrF9JD8s130_assertion a np:Assertion .
  
  dgn-np:NP548597.RAD-3bsh8jGkAIauE7QpkwmqbUuAkQUEdeA_aDrF9JD8s130_provenance a np:Provenance .
  
  dgn-np:NP548597.RAD-3bsh8jGkAIauE7QpkwmqbUuAkQUEdeA_aDrF9JD8s130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP548597.RAD-3bsh8jGkAIauE7QpkwmqbUuAkQUEdeA_aDrF9JD8s130_assertion {
  miriam-gene:2739 a ncit:C16612 .
  
  lld:C0403396 a ncit:C7057 .
  
  dgn-gda:DGN09ec85d236b699422116f448172a5972 sio:SIO_000628 miriam-gene:2739, lld:C0403396;
    a sio:SIO_001121 .
}

dgn-np:NP548597.RAD-3bsh8jGkAIauE7QpkwmqbUuAkQUEdeA_aDrF9JD8s130_provenance {
  dgn-np:NP548597.RAD-3bsh8jGkAIauE7QpkwmqbUuAkQUEdeA_aDrF9JD8s130_assertion dcterms:description
      "[To determine whether steroid-sensitive nephrotic syndrome is associated with greater than expected frequencies of specific extended haplotypes of the major histocompatibility complex, we studied genetic markers (Class I, II, III HLA alleles and glyoxalase I) in 173 subjects in 42 families of patients with nephrotic syndrome of childhood.]. 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:1974661;
    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:NP548597.RAD-3bsh8jGkAIauE7QpkwmqbUuAkQUEdeA_aDrF9JD8s130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:30+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" .
}