@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP928246.RAE7J6ZHxoqRbHWemZl20ZOFZQ0-CFnMIOnevGTU42hj0> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP928246.RAE7J6ZHxoqRbHWemZl20ZOFZQ0-CFnMIOnevGTU42hj0130_head {
   this: np:hasAssertion dgn-np:NP928246.RAE7J6ZHxoqRbHWemZl20ZOFZQ0-CFnMIOnevGTU42hj0130_assertion ;
    np:hasProvenance dgn-np:NP928246.RAE7J6ZHxoqRbHWemZl20ZOFZQ0-CFnMIOnevGTU42hj0130_provenance ;
    np:hasPublicationInfo dgn-np:NP928246.RAE7J6ZHxoqRbHWemZl20ZOFZQ0-CFnMIOnevGTU42hj0130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP928246.RAE7J6ZHxoqRbHWemZl20ZOFZQ0-CFnMIOnevGTU42hj0130_provenance a np:Provenance .
  dgn-np:NP928246.RAE7J6ZHxoqRbHWemZl20ZOFZQ0-CFnMIOnevGTU42hj0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP928246.RAE7J6ZHxoqRbHWemZl20ZOFZQ0-CFnMIOnevGTU42hj0130_assertion {
   miriam-gene:8542 a ncit:C16612 .
  lld:C0022658 a ncit:C7057 .
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    a sio:SIO_001121 .
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dgn-np:NP928246.RAE7J6ZHxoqRbHWemZl20ZOFZQ0-CFnMIOnevGTU42hj0130_provenance {
   dgn-np:NP928246.RAE7J6ZHxoqRbHWemZl20ZOFZQ0-CFnMIOnevGTU42hj0130_assertion dcterms:description "[We determined the frequency of the APOL1 G1 and G2 risk variants together with the prevalence of HIV-associated nephropathy (HIVAN) among individuals of Ethiopian ancestry to determine whether the kidney disease genetic risk is PanAfrican or restricted to West Africa, and can explain the previously reported low risk of HIVAN among Ethiopians.]. 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:21968148 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date .
  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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}
dgn-np:NP928246.RAE7J6ZHxoqRbHWemZl20ZOFZQ0-CFnMIOnevGTU42hj0130_publicationInfo {
   this: dcterms:created "2016-05-13T12:48:45+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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    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> ;
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}