@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP577434.RATv_f-E5wtbF6gyqESBQs3h0Ds1geHqhQXNo7ayOVElI> .
@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:NP577434.RATv_f-E5wtbF6gyqESBQs3h0Ds1geHqhQXNo7ayOVElI130_head {
  this: np:hasAssertion dgn-np:NP577434.RATv_f-E5wtbF6gyqESBQs3h0Ds1geHqhQXNo7ayOVElI130_assertion ;
    np:hasProvenance dgn-np:NP577434.RATv_f-E5wtbF6gyqESBQs3h0Ds1geHqhQXNo7ayOVElI130_provenance ;
    np:hasPublicationInfo dgn-np:NP577434.RATv_f-E5wtbF6gyqESBQs3h0Ds1geHqhQXNo7ayOVElI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP577434.RATv_f-E5wtbF6gyqESBQs3h0Ds1geHqhQXNo7ayOVElI130_assertion a np:Assertion .
  dgn-np:NP577434.RATv_f-E5wtbF6gyqESBQs3h0Ds1geHqhQXNo7ayOVElI130_provenance a np:Provenance .
  dgn-np:NP577434.RATv_f-E5wtbF6gyqESBQs3h0Ds1geHqhQXNo7ayOVElI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP577434.RATv_f-E5wtbF6gyqESBQs3h0Ds1geHqhQXNo7ayOVElI130_assertion {
  miriam-gene:23771 a ncit:C16612 .
  lld:C0022658 a ncit:C7057 .
  dgn-gda:DGNd3330eb707c70696a0ce705f98bdb200 sio:SIO_000628 miriam-gene:23771 , lld:C0022658 ;
    a sio:SIO_001121 .
}
dgn-np:NP577434.RATv_f-E5wtbF6gyqESBQs3h0Ds1geHqhQXNo7ayOVElI130_provenance {
  dgn-np:NP577434.RATv_f-E5wtbF6gyqESBQs3h0Ds1geHqhQXNo7ayOVElI130_assertion dcterms:description "[Although genes have not been definitely linked to renal vascular disease, population- and family-based epidemiology of kidney disease, segregation analysis of Pima and Caucasian families in which diabetic nephropathy is clustered, and the positional cloning of genes responsible for rare, familial glomerulosclerosis syndromes support the hypothesis that genes regulate the pathogenesis of renal disease.]. 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:12496669 ;
    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:NP577434.RATv_f-E5wtbF6gyqESBQs3h0Ds1geHqhQXNo7ayOVElI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:48+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> , <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" .
}