@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP96050.RABJDzVLWJGGoQLDxLsLnB65yx1FdiitW8fUocm1r1iek> .
@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:NP96050.RABJDzVLWJGGoQLDxLsLnB65yx1FdiitW8fUocm1r1iek130_head {
  this: np:hasAssertion dgn-np:NP96050.RABJDzVLWJGGoQLDxLsLnB65yx1FdiitW8fUocm1r1iek130_assertion;
    np:hasProvenance dgn-np:NP96050.RABJDzVLWJGGoQLDxLsLnB65yx1FdiitW8fUocm1r1iek130_provenance;
    np:hasPublicationInfo dgn-np:NP96050.RABJDzVLWJGGoQLDxLsLnB65yx1FdiitW8fUocm1r1iek130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP96050.RABJDzVLWJGGoQLDxLsLnB65yx1FdiitW8fUocm1r1iek130_assertion a np:Assertion .
  
  dgn-np:NP96050.RABJDzVLWJGGoQLDxLsLnB65yx1FdiitW8fUocm1r1iek130_provenance a np:Provenance .
  
  dgn-np:NP96050.RABJDzVLWJGGoQLDxLsLnB65yx1FdiitW8fUocm1r1iek130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP96050.RABJDzVLWJGGoQLDxLsLnB65yx1FdiitW8fUocm1r1iek130_assertion {
  miriam-gene:5797 a ncit:C16612 .
  
  lld:C0011860 a ncit:C7057 .
  
  dgn-gda:DGN05d1f6ffcdbd297bdb4e7f98984fba04 sio:SIO_000628 miriam-gene:5797, lld:C0011860;
    a sio:SIO_001122 .
}

dgn-np:NP96050.RABJDzVLWJGGoQLDxLsLnB65yx1FdiitW8fUocm1r1iek130_provenance {
  dgn-np:NP96050.RABJDzVLWJGGoQLDxLsLnB65yx1FdiitW8fUocm1r1iek130_assertion dcterms:description
      "[Genetic variation may modify the risk of death on dialysis. SNPs in proximity to genes regulating vascular extracellular matrix, cardiac ventricular repolarization, and smoking cessation are associated with dialysis survival in AAs with T2D. These results warrant replication in other cohorts and races.]. 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:21546767;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP96050.RABJDzVLWJGGoQLDxLsLnB65yx1FdiitW8fUocm1r1iek130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:48+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}