@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP584843.RAlPyzA9jkPejgAe04TRC7atl4-kiEWpWpnszGnxvaFFE> .
@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:NP584843.RAlPyzA9jkPejgAe04TRC7atl4-kiEWpWpnszGnxvaFFE130_head {
  this: np:hasAssertion dgn-np:NP584843.RAlPyzA9jkPejgAe04TRC7atl4-kiEWpWpnszGnxvaFFE130_assertion;
    np:hasProvenance dgn-np:NP584843.RAlPyzA9jkPejgAe04TRC7atl4-kiEWpWpnszGnxvaFFE130_provenance;
    np:hasPublicationInfo dgn-np:NP584843.RAlPyzA9jkPejgAe04TRC7atl4-kiEWpWpnszGnxvaFFE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP584843.RAlPyzA9jkPejgAe04TRC7atl4-kiEWpWpnszGnxvaFFE130_assertion a np:Assertion .
  
  dgn-np:NP584843.RAlPyzA9jkPejgAe04TRC7atl4-kiEWpWpnszGnxvaFFE130_provenance a np:Provenance .
  
  dgn-np:NP584843.RAlPyzA9jkPejgAe04TRC7atl4-kiEWpWpnszGnxvaFFE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP584843.RAlPyzA9jkPejgAe04TRC7atl4-kiEWpWpnszGnxvaFFE130_assertion {
  miriam-gene:941 a ncit:C16612 .
  
  lld:C1704320 a ncit:C7057 .
  
  dgn-gda:DGN1e4b4e91b597717246627f6958feb68f sio:SIO_000628 miriam-gene:941, lld:C1704320;
    a sio:SIO_001121 .
}

dgn-np:NP584843.RAlPyzA9jkPejgAe04TRC7atl4-kiEWpWpnszGnxvaFFE130_provenance {
  dgn-np:NP584843.RAlPyzA9jkPejgAe04TRC7atl4-kiEWpWpnszGnxvaFFE130_assertion dcterms:description
      "[Minimal change disease (MCD) is the most common cause of nephrotic syndrome in children and is associated with the expression of CD80 in podocytes and the increased excretion of CD80 in urine.]. 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:23689904;
    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:NP584843.RAlPyzA9jkPejgAe04TRC7atl4-kiEWpWpnszGnxvaFFE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:52+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" .
}