@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP717634.RAfHgn_gaSBwOir19_9heNQMvaf-hrPlb1MxsR6dFteqk> .
@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:NP717634.RAfHgn_gaSBwOir19_9heNQMvaf-hrPlb1MxsR6dFteqk130_head {
  this: np:hasAssertion dgn-np:NP717634.RAfHgn_gaSBwOir19_9heNQMvaf-hrPlb1MxsR6dFteqk130_assertion ;
    np:hasProvenance dgn-np:NP717634.RAfHgn_gaSBwOir19_9heNQMvaf-hrPlb1MxsR6dFteqk130_provenance ;
    np:hasPublicationInfo dgn-np:NP717634.RAfHgn_gaSBwOir19_9heNQMvaf-hrPlb1MxsR6dFteqk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP717634.RAfHgn_gaSBwOir19_9heNQMvaf-hrPlb1MxsR6dFteqk130_assertion a np:Assertion .
  dgn-np:NP717634.RAfHgn_gaSBwOir19_9heNQMvaf-hrPlb1MxsR6dFteqk130_provenance a np:Provenance .
  dgn-np:NP717634.RAfHgn_gaSBwOir19_9heNQMvaf-hrPlb1MxsR6dFteqk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP717634.RAfHgn_gaSBwOir19_9heNQMvaf-hrPlb1MxsR6dFteqk130_assertion {
  miriam-gene:338 a ncit:C16612 .
  lld:C1704436 a ncit:C7057 .
  dgn-gda:DGN0133091152b97075e83039a0c1994ecf sio:SIO_000628 miriam-gene:338 , lld:C1704436 ;
    a sio:SIO_001121 .
}
dgn-np:NP717634.RAfHgn_gaSBwOir19_9heNQMvaf-hrPlb1MxsR6dFteqk130_provenance {
  dgn-np:NP717634.RAfHgn_gaSBwOir19_9heNQMvaf-hrPlb1MxsR6dFteqk130_assertion dcterms:description "[Our observations suggest that variation in the apolipoprotein AI-CIII-AIV gene cluster may not be contributing significantly to the development of peripheral arterial disease, but variation associated with some of the restriction fragment length polymorphisms may be involved in determining levels of cholesterol- and apolipoprotein-B-containing lipoproteins.]. 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:2564329 ;
    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:NP717634.RAfHgn_gaSBwOir19_9heNQMvaf-hrPlb1MxsR6dFteqk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:15+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" .
}