@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP535742.RABoZY4nhdOJ0bLYzCcultD1nWMX5eHf-8m-pJFITuPIE> .
@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:NP535742.RABoZY4nhdOJ0bLYzCcultD1nWMX5eHf-8m-pJFITuPIE130_head {
  this: np:hasAssertion dgn-np:NP535742.RABoZY4nhdOJ0bLYzCcultD1nWMX5eHf-8m-pJFITuPIE130_assertion;
    np:hasProvenance dgn-np:NP535742.RABoZY4nhdOJ0bLYzCcultD1nWMX5eHf-8m-pJFITuPIE130_provenance;
    np:hasPublicationInfo dgn-np:NP535742.RABoZY4nhdOJ0bLYzCcultD1nWMX5eHf-8m-pJFITuPIE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP535742.RABoZY4nhdOJ0bLYzCcultD1nWMX5eHf-8m-pJFITuPIE130_assertion a np:Assertion .
  
  dgn-np:NP535742.RABoZY4nhdOJ0bLYzCcultD1nWMX5eHf-8m-pJFITuPIE130_provenance a np:Provenance .
  
  dgn-np:NP535742.RABoZY4nhdOJ0bLYzCcultD1nWMX5eHf-8m-pJFITuPIE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP535742.RABoZY4nhdOJ0bLYzCcultD1nWMX5eHf-8m-pJFITuPIE130_assertion {
  miriam-gene:7124 a ncit:C16612 .
  
  lld:C0011881 a ncit:C7057 .
  
  dgn-gda:DGNa32f9f9571d147715eae297f1504905f sio:SIO_000628 miriam-gene:7124, lld:C0011881;
    a sio:SIO_001121 .
}

dgn-np:NP535742.RABoZY4nhdOJ0bLYzCcultD1nWMX5eHf-8m-pJFITuPIE130_provenance {
  dgn-np:NP535742.RABoZY4nhdOJ0bLYzCcultD1nWMX5eHf-8m-pJFITuPIE130_assertion dcterms:description
      "[In conclusion, we found that in diabetic nephropathy patients molecular variants of TNF are more frequent than in nondiabetic patients with chronic renal failure and these changes might be associated with altered ability to TNF synthesis.]. 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:15600254;
    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:NP535742.RABoZY4nhdOJ0bLYzCcultD1nWMX5eHf-8m-pJFITuPIE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:23+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" .
}