@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1014848.RAEwFGImvBmv2gxkPzk5Rq8230GlheTpri_Ok5bGCdwFY> .
@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/v4.0.0/void/> .
dgn-np:NP1014848.RAEwFGImvBmv2gxkPzk5Rq8230GlheTpri_Ok5bGCdwFY130_head {
   this: np:hasAssertion dgn-np:NP1014848.RAEwFGImvBmv2gxkPzk5Rq8230GlheTpri_Ok5bGCdwFY130_assertion ;
    np:hasProvenance dgn-np:NP1014848.RAEwFGImvBmv2gxkPzk5Rq8230GlheTpri_Ok5bGCdwFY130_provenance ;
    np:hasPublicationInfo dgn-np:NP1014848.RAEwFGImvBmv2gxkPzk5Rq8230GlheTpri_Ok5bGCdwFY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1014848.RAEwFGImvBmv2gxkPzk5Rq8230GlheTpri_Ok5bGCdwFY130_assertion a np:Assertion .
  dgn-np:NP1014848.RAEwFGImvBmv2gxkPzk5Rq8230GlheTpri_Ok5bGCdwFY130_provenance a np:Provenance .
  dgn-np:NP1014848.RAEwFGImvBmv2gxkPzk5Rq8230GlheTpri_Ok5bGCdwFY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1014848.RAEwFGImvBmv2gxkPzk5Rq8230GlheTpri_Ok5bGCdwFY130_assertion {
   miriam-gene:4018 a ncit:C16612 .
  lld:C0010068 a ncit:C7057 .
  dgn-gda:DGN32716eb7de54eef31c95f86bdb28677a sio:SIO_000628 miriam-gene:4018 , lld:C0010068 ;
    a sio:SIO_001121 .
}
dgn-np:NP1014848.RAEwFGImvBmv2gxkPzk5Rq8230GlheTpri_Ok5bGCdwFY130_provenance {
   dgn-np:NP1014848.RAEwFGImvBmv2gxkPzk5Rq8230GlheTpri_Ok5bGCdwFY130_assertion dcterms:description "[The copy number variation of kringle IV in the LPA gene has been strongly associated with both Lp(a) levels in plasma and risk of CHD, thereby fulfilling the main criterion for causality in a Mendelian randomization approach.]. 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:22998429 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1014848.RAEwFGImvBmv2gxkPzk5Rq8230GlheTpri_Ok5bGCdwFY130_publicationInfo {
   this: dcterms:created "2016-05-13T12:49:26+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}