@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP785758.RAvT-JeXeShLnzPTV4BDwQrSPn4MFHqC9qwgkC2uVEBA8> .
@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/v3.0.0/void/> .
dgn-np:NP785758.RAvT-JeXeShLnzPTV4BDwQrSPn4MFHqC9qwgkC2uVEBA8130_head {
  this: np:hasAssertion dgn-np:NP785758.RAvT-JeXeShLnzPTV4BDwQrSPn4MFHqC9qwgkC2uVEBA8130_assertion ;
    np:hasProvenance dgn-np:NP785758.RAvT-JeXeShLnzPTV4BDwQrSPn4MFHqC9qwgkC2uVEBA8130_provenance ;
    np:hasPublicationInfo dgn-np:NP785758.RAvT-JeXeShLnzPTV4BDwQrSPn4MFHqC9qwgkC2uVEBA8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP785758.RAvT-JeXeShLnzPTV4BDwQrSPn4MFHqC9qwgkC2uVEBA8130_assertion a np:Assertion .
  dgn-np:NP785758.RAvT-JeXeShLnzPTV4BDwQrSPn4MFHqC9qwgkC2uVEBA8130_provenance a np:Provenance .
  dgn-np:NP785758.RAvT-JeXeShLnzPTV4BDwQrSPn4MFHqC9qwgkC2uVEBA8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP785758.RAvT-JeXeShLnzPTV4BDwQrSPn4MFHqC9qwgkC2uVEBA8130_assertion {
  miriam-gene:7903 a ncit:C16612 .
  lld:C0038454 a ncit:C7057 .
  dgn-gda:DGNc7d11a6e48b645c1cdea1d92a88a6748 sio:SIO_000628 miriam-gene:7903 , lld:C0038454 ;
    a sio:SIO_001121 .
}
dgn-np:NP785758.RAvT-JeXeShLnzPTV4BDwQrSPn4MFHqC9qwgkC2uVEBA8130_provenance {
  dgn-np:NP785758.RAvT-JeXeShLnzPTV4BDwQrSPn4MFHqC9qwgkC2uVEBA8130_assertion dcterms:description "[Restriction fragment length polymorphism of the apolipoprotein AI gene, which encodes the most prominent apoproteins in high density lipoprotein (HDL), were investigated using the restriction enzymes Sac I and Pst I in white and black subjects to determine the potential role of genetic variations as stroke risks as determined by carotid stenosis and an atherogenic serum profile, such as elevated total cholesterol and low density lipoprotein (LDL) levels or reduced HDL levels.]. 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:8249016 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP785758.RAvT-JeXeShLnzPTV4BDwQrSPn4MFHqC9qwgkC2uVEBA8130_publicationInfo {
  this: dcterms:created "2015-08-25T14:45:35+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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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> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v3.0.0.0" .
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}