@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP508102.RAQKSrmi1aEa_A0Qw_bfNyH_DSoFVgB5D0GcTLzxJtVSM> .
@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:NP508102.RAQKSrmi1aEa_A0Qw_bfNyH_DSoFVgB5D0GcTLzxJtVSM130_head {
  this: np:hasAssertion dgn-np:NP508102.RAQKSrmi1aEa_A0Qw_bfNyH_DSoFVgB5D0GcTLzxJtVSM130_assertion ;
    np:hasProvenance dgn-np:NP508102.RAQKSrmi1aEa_A0Qw_bfNyH_DSoFVgB5D0GcTLzxJtVSM130_provenance ;
    np:hasPublicationInfo dgn-np:NP508102.RAQKSrmi1aEa_A0Qw_bfNyH_DSoFVgB5D0GcTLzxJtVSM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP508102.RAQKSrmi1aEa_A0Qw_bfNyH_DSoFVgB5D0GcTLzxJtVSM130_assertion a np:Assertion .
  dgn-np:NP508102.RAQKSrmi1aEa_A0Qw_bfNyH_DSoFVgB5D0GcTLzxJtVSM130_provenance a np:Provenance .
  dgn-np:NP508102.RAQKSrmi1aEa_A0Qw_bfNyH_DSoFVgB5D0GcTLzxJtVSM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP508102.RAQKSrmi1aEa_A0Qw_bfNyH_DSoFVgB5D0GcTLzxJtVSM130_assertion {
  miriam-gene:4358 a ncit:C16612 .
  lld:C0017668 a ncit:C7057 .
  dgn-gda:DGN0a7d07d90470aed83adceb67be6a970b sio:SIO_000628 miriam-gene:4358 , lld:C0017668 ;
    a sio:SIO_001121 .
}
dgn-np:NP508102.RAQKSrmi1aEa_A0Qw_bfNyH_DSoFVgB5D0GcTLzxJtVSM130_provenance {
  dgn-np:NP508102.RAQKSrmi1aEa_A0Qw_bfNyH_DSoFVgB5D0GcTLzxJtVSM130_assertion dcterms:description "[The frequency of this haplotype in the Australian dialysis and transplant population with focal glomerulosclerosis was compared to that seen in the general Australian Caucasian population and was not significantly different suggesting that the presence of the HLA alleles HLA-A1, B8, DR3, DR7 may increase the predisposition to familial glomerulosclerosis but additional factors are required for disease development and progression.]. 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:7503147 ;
    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:NP508102.RAQKSrmi1aEa_A0Qw_bfNyH_DSoFVgB5D0GcTLzxJtVSM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:03+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" .
}