@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP472185.RAJALbiLX4qoRFvpGCd4GHa0pu0suCXOal1AjAPhgqVBk> .
@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:NP472185.RAJALbiLX4qoRFvpGCd4GHa0pu0suCXOal1AjAPhgqVBk130_head {
  this: np:hasAssertion dgn-np:NP472185.RAJALbiLX4qoRFvpGCd4GHa0pu0suCXOal1AjAPhgqVBk130_assertion;
    np:hasProvenance dgn-np:NP472185.RAJALbiLX4qoRFvpGCd4GHa0pu0suCXOal1AjAPhgqVBk130_provenance;
    np:hasPublicationInfo dgn-np:NP472185.RAJALbiLX4qoRFvpGCd4GHa0pu0suCXOal1AjAPhgqVBk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP472185.RAJALbiLX4qoRFvpGCd4GHa0pu0suCXOal1AjAPhgqVBk130_assertion a np:Assertion .
  
  dgn-np:NP472185.RAJALbiLX4qoRFvpGCd4GHa0pu0suCXOal1AjAPhgqVBk130_provenance a np:Provenance .
  
  dgn-np:NP472185.RAJALbiLX4qoRFvpGCd4GHa0pu0suCXOal1AjAPhgqVBk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP472185.RAJALbiLX4qoRFvpGCd4GHa0pu0suCXOal1AjAPhgqVBk130_assertion {
  miriam-gene:3308 a ncit:C16612 .
  
  lld:C0282666 a ncit:C7057 .
  
  dgn-gda:DGN01a26d5663eb18183ca07b3f4b15e6f6 sio:SIO_000628 miriam-gene:3308, lld:C0282666;
    a sio:SIO_001121 .
}

dgn-np:NP472185.RAJALbiLX4qoRFvpGCd4GHa0pu0suCXOal1AjAPhgqVBk130_provenance {
  dgn-np:NP472185.RAJALbiLX4qoRFvpGCd4GHa0pu0suCXOal1AjAPhgqVBk130_assertion dcterms:description
      "[We have investigated the association of genetic polymorphisms of the constitutive HSP70 (HSP73) and the inducible HSP70 (HSP72) encoding genes with the risk of acute renal failure (ARF) in very low birth weight (VLBW) neonates.]. 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:12840151;
    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:NP472185.RAJALbiLX4qoRFvpGCd4GHa0pu0suCXOal1AjAPhgqVBk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:43+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" .
}