@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP96055.RAR106U-QUdw0ZOHiVzL6ycal_bR6iR34NjEnmb0HXiZo> .
@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 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:NP96055.RAR106U-QUdw0ZOHiVzL6ycal_bR6iR34NjEnmb0HXiZo130_head {
  this: np:hasAssertion dgn-np:NP96055.RAR106U-QUdw0ZOHiVzL6ycal_bR6iR34NjEnmb0HXiZo130_assertion ;
    np:hasProvenance dgn-np:NP96055.RAR106U-QUdw0ZOHiVzL6ycal_bR6iR34NjEnmb0HXiZo130_provenance ;
    np:hasPublicationInfo dgn-np:NP96055.RAR106U-QUdw0ZOHiVzL6ycal_bR6iR34NjEnmb0HXiZo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP96055.RAR106U-QUdw0ZOHiVzL6ycal_bR6iR34NjEnmb0HXiZo130_assertion a np:Assertion .
  dgn-np:NP96055.RAR106U-QUdw0ZOHiVzL6ycal_bR6iR34NjEnmb0HXiZo130_provenance a np:Provenance .
  dgn-np:NP96055.RAR106U-QUdw0ZOHiVzL6ycal_bR6iR34NjEnmb0HXiZo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP96055.RAR106U-QUdw0ZOHiVzL6ycal_bR6iR34NjEnmb0HXiZo130_assertion {
  miriam-gene:258010 a ncit:C16612 .
  lld:C0011860 a ncit:C7057 .
  dgn-gda:DGN4306982db1c715a758498f8042380322 sio:SIO_000628 miriam-gene:258010 , lld:C0011860 ;
    a sio:SIO_001122 .
}
dgn-np:NP96055.RAR106U-QUdw0ZOHiVzL6ycal_bR6iR34NjEnmb0HXiZo130_provenance {
  dgn-np:NP96055.RAR106U-QUdw0ZOHiVzL6ycal_bR6iR34NjEnmb0HXiZo130_assertion dc: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:NP96055.RAR106U-QUdw0ZOHiVzL6ycal_bR6iR34NjEnmb0HXiZo130_publicationInfo {
  this: dc:created "2014-10-02T12:32:48+02:00"^^xsd:dateTime ;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dc:rightsHolder dgn-void:IBIGroup ;
    dc: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" .
}