@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP82893.RAqHAALytxaPKoarF7MOWF6aiYZP2Z6ju2iBi0H1Hg4pg> .
@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:NP82893.RAqHAALytxaPKoarF7MOWF6aiYZP2Z6ju2iBi0H1Hg4pg130_head {
  this: np:hasAssertion dgn-np:NP82893.RAqHAALytxaPKoarF7MOWF6aiYZP2Z6ju2iBi0H1Hg4pg130_assertion;
    np:hasProvenance dgn-np:NP82893.RAqHAALytxaPKoarF7MOWF6aiYZP2Z6ju2iBi0H1Hg4pg130_provenance;
    np:hasPublicationInfo dgn-np:NP82893.RAqHAALytxaPKoarF7MOWF6aiYZP2Z6ju2iBi0H1Hg4pg130_publicationInfo;
    a np:Nanopublication .
  
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  dgn-np:NP82893.RAqHAALytxaPKoarF7MOWF6aiYZP2Z6ju2iBi0H1Hg4pg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP82893.RAqHAALytxaPKoarF7MOWF6aiYZP2Z6ju2iBi0H1Hg4pg130_assertion {
  miriam-gene:8542 a ncit:C16612 .
  
  lld:C0022658 a ncit:C7057 .
  
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    a sio:SIO_001122 .
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dgn-np:NP82893.RAqHAALytxaPKoarF7MOWF6aiYZP2Z6ju2iBi0H1Hg4pg130_provenance {
  dgn-np:NP82893.RAqHAALytxaPKoarF7MOWF6aiYZP2Z6ju2iBi0H1Hg4pg130_assertion dcterms:description
      "[We also show that the distribution of these newly identified APOL1 risk variants in African populations is consistent with the pattern of African ancestry ESKD risk previously attributed to MYH9.Mapping by admixture linkage disequilibrium (MALD) localized an interval on chromosome 22, in a region that includes the MYH9 gene, which was shown to contain African ancestry risk variants associated with certain forms of ESKD (Kao et al.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    prov:wasDerivedFrom dgn-void:gad-20130706;
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  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 .
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dgn-np:NP82893.RAqHAALytxaPKoarF7MOWF6aiYZP2Z6ju2iBi0H1Hg4pg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:41+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;
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      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
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    pav:version "v2.1.0.0" .
  
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