@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP439460.RAYI4L6Zr3OEOakmI8UDMS0F4vJ_H3wGltDJhHchH8oRo> .
@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:NP439460.RAYI4L6Zr3OEOakmI8UDMS0F4vJ_H3wGltDJhHchH8oRo130_head {
  this: np:hasAssertion dgn-np:NP439460.RAYI4L6Zr3OEOakmI8UDMS0F4vJ_H3wGltDJhHchH8oRo130_assertion;
    np:hasProvenance dgn-np:NP439460.RAYI4L6Zr3OEOakmI8UDMS0F4vJ_H3wGltDJhHchH8oRo130_provenance;
    np:hasPublicationInfo dgn-np:NP439460.RAYI4L6Zr3OEOakmI8UDMS0F4vJ_H3wGltDJhHchH8oRo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP439460.RAYI4L6Zr3OEOakmI8UDMS0F4vJ_H3wGltDJhHchH8oRo130_assertion a np:Assertion .
  
  dgn-np:NP439460.RAYI4L6Zr3OEOakmI8UDMS0F4vJ_H3wGltDJhHchH8oRo130_provenance a np:Provenance .
  
  dgn-np:NP439460.RAYI4L6Zr3OEOakmI8UDMS0F4vJ_H3wGltDJhHchH8oRo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP439460.RAYI4L6Zr3OEOakmI8UDMS0F4vJ_H3wGltDJhHchH8oRo130_assertion {
  miriam-gene:23771 a ncit:C16612 .
  
  lld:C0264657 a ncit:C7057 .
  
  dgn-gda:DGNa70261f0a60ea8e10525ca85bccdfd7a sio:SIO_000628 miriam-gene:23771, lld:C0264657;
    a sio:SIO_001121 .
}

dgn-np:NP439460.RAYI4L6Zr3OEOakmI8UDMS0F4vJ_H3wGltDJhHchH8oRo130_provenance {
  dgn-np:NP439460.RAYI4L6Zr3OEOakmI8UDMS0F4vJ_H3wGltDJhHchH8oRo130_assertion dcterms:description
      "[Genotyping the -463G/A polymorphism in HN, chronic glomerulonephritis (CGN) and diabetic nephropathy (DM) patients who were under hemodialysis treatment demonstrated that the GG genotype was more frequent in the HN group than in the CGN and DM groups.]. 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:18344624;
    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:NP439460.RAYI4L6Zr3OEOakmI8UDMS0F4vJ_H3wGltDJhHchH8oRo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:20+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" .
}