@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP303522.RAW8yohrQThkBXx9i5wgY0N-YSnG-N17HOWZw3lk9bpE0> .
@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:NP303522.RAW8yohrQThkBXx9i5wgY0N-YSnG-N17HOWZw3lk9bpE0130_head {
  this: np:hasAssertion dgn-np:NP303522.RAW8yohrQThkBXx9i5wgY0N-YSnG-N17HOWZw3lk9bpE0130_assertion ;
    np:hasProvenance dgn-np:NP303522.RAW8yohrQThkBXx9i5wgY0N-YSnG-N17HOWZw3lk9bpE0130_provenance ;
    np:hasPublicationInfo dgn-np:NP303522.RAW8yohrQThkBXx9i5wgY0N-YSnG-N17HOWZw3lk9bpE0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP303522.RAW8yohrQThkBXx9i5wgY0N-YSnG-N17HOWZw3lk9bpE0130_assertion a np:Assertion .
  dgn-np:NP303522.RAW8yohrQThkBXx9i5wgY0N-YSnG-N17HOWZw3lk9bpE0130_provenance a np:Provenance .
  dgn-np:NP303522.RAW8yohrQThkBXx9i5wgY0N-YSnG-N17HOWZw3lk9bpE0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP303522.RAW8yohrQThkBXx9i5wgY0N-YSnG-N17HOWZw3lk9bpE0130_assertion {
  miriam-gene:8542 a ncit:C16612 .
  lld:C0078911 a ncit:C7057 .
  dgn-gda:DGNcde3c5a727d436017a33b2ae155b128d sio:SIO_000628 miriam-gene:8542 , lld:C0078911 ;
    a sio:SIO_001121 .
}
dgn-np:NP303522.RAW8yohrQThkBXx9i5wgY0N-YSnG-N17HOWZw3lk9bpE0130_provenance {
  dgn-np:NP303522.RAW8yohrQThkBXx9i5wgY0N-YSnG-N17HOWZw3lk9bpE0130_assertion dcterms:description "[Thus, our study suggests that although the majority of African-American patients with HIVAN have two APOL1 risk alleles other as yet unknown factors in the host, including genetic risk variants and environmental or viral factors, may influence the development of this disorder in those with zero or one APOL1 risk allele.]. 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:22495294 ;
    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:NP303522.RAW8yohrQThkBXx9i5wgY0N-YSnG-N17HOWZw3lk9bpE0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:54+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" .
}