@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP895930.RA2l7vB9sv98xh8keh82vPq-FxVsCthfk7WKSTRBW6y8o> .
@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:NP895930.RA2l7vB9sv98xh8keh82vPq-FxVsCthfk7WKSTRBW6y8o130_head {
  this: np:hasAssertion dgn-np:NP895930.RA2l7vB9sv98xh8keh82vPq-FxVsCthfk7WKSTRBW6y8o130_assertion;
    np:hasProvenance dgn-np:NP895930.RA2l7vB9sv98xh8keh82vPq-FxVsCthfk7WKSTRBW6y8o130_provenance;
    np:hasPublicationInfo dgn-np:NP895930.RA2l7vB9sv98xh8keh82vPq-FxVsCthfk7WKSTRBW6y8o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP895930.RA2l7vB9sv98xh8keh82vPq-FxVsCthfk7WKSTRBW6y8o130_assertion a np:Assertion .
  
  dgn-np:NP895930.RA2l7vB9sv98xh8keh82vPq-FxVsCthfk7WKSTRBW6y8o130_provenance a np:Provenance .
  
  dgn-np:NP895930.RA2l7vB9sv98xh8keh82vPq-FxVsCthfk7WKSTRBW6y8o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP895930.RA2l7vB9sv98xh8keh82vPq-FxVsCthfk7WKSTRBW6y8o130_assertion {
  miriam-gene:213 a ncit:C16612 .
  
  lld:C0027726 a ncit:C7057 .
  
  dgn-gda:DGN09539918ae35da87789db30f81d9383d sio:SIO_000628 miriam-gene:213, lld:C0027726;
    a sio:SIO_001121 .
}

dgn-np:NP895930.RA2l7vB9sv98xh8keh82vPq-FxVsCthfk7WKSTRBW6y8o130_provenance {
  dgn-np:NP895930.RA2l7vB9sv98xh8keh82vPq-FxVsCthfk7WKSTRBW6y8o130_assertion dcterms:description
      "[In both the nephrotic syndrome (NS) and hereditary analbuminemia in the Nagase analbuminemic rat (NAR), the plasma protein concentration is nearly normal since albumin is replaced by several high molecular weight proteins.]. 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:9453001;
    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:NP895930.RA2l7vB9sv98xh8keh82vPq-FxVsCthfk7WKSTRBW6y8o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:10+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" .
}