@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP700568.RA9AKrDYCvL9CXF3uR0nOBx0PNL6emmNUpKSoKVS2YGVQ> .
@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:NP700568.RA9AKrDYCvL9CXF3uR0nOBx0PNL6emmNUpKSoKVS2YGVQ130_head {
  this: np:hasAssertion dgn-np:NP700568.RA9AKrDYCvL9CXF3uR0nOBx0PNL6emmNUpKSoKVS2YGVQ130_assertion ;
    np:hasProvenance dgn-np:NP700568.RA9AKrDYCvL9CXF3uR0nOBx0PNL6emmNUpKSoKVS2YGVQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP700568.RA9AKrDYCvL9CXF3uR0nOBx0PNL6emmNUpKSoKVS2YGVQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP700568.RA9AKrDYCvL9CXF3uR0nOBx0PNL6emmNUpKSoKVS2YGVQ130_assertion a np:Assertion .
  dgn-np:NP700568.RA9AKrDYCvL9CXF3uR0nOBx0PNL6emmNUpKSoKVS2YGVQ130_provenance a np:Provenance .
  dgn-np:NP700568.RA9AKrDYCvL9CXF3uR0nOBx0PNL6emmNUpKSoKVS2YGVQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP700568.RA9AKrDYCvL9CXF3uR0nOBx0PNL6emmNUpKSoKVS2YGVQ130_assertion {
  miriam-gene:127062 a ncit:C16612 .
  lld:C0022661 a ncit:C7057 .
  dgn-gda:DGN455faf94d721ac757f8db4ae109124a2 sio:SIO_000628 miriam-gene:127062 , lld:C0022661 ;
    a sio:SIO_001121 .
}
dgn-np:NP700568.RA9AKrDYCvL9CXF3uR0nOBx0PNL6emmNUpKSoKVS2YGVQ130_provenance {
  dgn-np:NP700568.RA9AKrDYCvL9CXF3uR0nOBx0PNL6emmNUpKSoKVS2YGVQ130_assertion dcterms:description "[Genotyping analysis demonstrated that 2 SNPs among 13 were significantly associated with ESRD after adjusting for age and sex, which were shown by IL17E rs10137082 (odds ratio (OR) 1.48 in codominant 1, OR 1.54 in dominant, OR 1.47 in log-additive) and IL17RA rs4819554 (OR 1.46 in codominant 1, OR 1.79 in codominant 2, OR 1.54 in dominant, OR 1.39 in log-additive).]. 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:23147652 ;
    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:NP700568.RA9AKrDYCvL9CXF3uR0nOBx0PNL6emmNUpKSoKVS2YGVQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:06+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" .
}