@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP841878.RAP1lbEJbVhDo_lWkc9M0bwJNLnh1m7paKXTR1iH8F84E> .
@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:NP841878.RAP1lbEJbVhDo_lWkc9M0bwJNLnh1m7paKXTR1iH8F84E130_head {
  this: np:hasAssertion dgn-np:NP841878.RAP1lbEJbVhDo_lWkc9M0bwJNLnh1m7paKXTR1iH8F84E130_assertion ;
    np:hasProvenance dgn-np:NP841878.RAP1lbEJbVhDo_lWkc9M0bwJNLnh1m7paKXTR1iH8F84E130_provenance ;
    np:hasPublicationInfo dgn-np:NP841878.RAP1lbEJbVhDo_lWkc9M0bwJNLnh1m7paKXTR1iH8F84E130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP841878.RAP1lbEJbVhDo_lWkc9M0bwJNLnh1m7paKXTR1iH8F84E130_assertion a np:Assertion .
  dgn-np:NP841878.RAP1lbEJbVhDo_lWkc9M0bwJNLnh1m7paKXTR1iH8F84E130_provenance a np:Provenance .
  dgn-np:NP841878.RAP1lbEJbVhDo_lWkc9M0bwJNLnh1m7paKXTR1iH8F84E130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP841878.RAP1lbEJbVhDo_lWkc9M0bwJNLnh1m7paKXTR1iH8F84E130_assertion {
  miriam-gene:116519 a ncit:C16612 .
  lld:C0038454 a ncit:C7057 .
  dgn-gda:DGN80ff5d69edecc1428444b9c41d77df45 sio:SIO_000628 miriam-gene:116519 , lld:C0038454 ;
    a sio:SIO_001121 .
}
dgn-np:NP841878.RAP1lbEJbVhDo_lWkc9M0bwJNLnh1m7paKXTR1iH8F84E130_provenance {
  dgn-np:NP841878.RAP1lbEJbVhDo_lWkc9M0bwJNLnh1m7paKXTR1iH8F84E130_assertion dcterms:description "[This pool of samples was previously investigated for haplotype tagging minor alleles of apolipoprotein A5 gene (T-1131C, T1259C, IVS3+G476A and C56G), and an association was found between the minor allele carriage and the triglyceride levels, and also these variants were found to confer risk to the development of stroke.]. 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:20158509 ;
    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:NP841878.RAP1lbEJbVhDo_lWkc9M0bwJNLnh1m7paKXTR1iH8F84E130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:34+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" .
}