@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1295040.RAg4UkZS4x4HYcGXpyVDAicwJ-imQXP9rV11ztkwPpH4c> .
@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:NP1295040.RAg4UkZS4x4HYcGXpyVDAicwJ-imQXP9rV11ztkwPpH4c130_head {
  this: np:hasAssertion dgn-np:NP1295040.RAg4UkZS4x4HYcGXpyVDAicwJ-imQXP9rV11ztkwPpH4c130_assertion;
    np:hasProvenance dgn-np:NP1295040.RAg4UkZS4x4HYcGXpyVDAicwJ-imQXP9rV11ztkwPpH4c130_provenance;
    np:hasPublicationInfo dgn-np:NP1295040.RAg4UkZS4x4HYcGXpyVDAicwJ-imQXP9rV11ztkwPpH4c130_publicationInfo;
    a np:Nanopublication .
  
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    a np:PublicationInfo .
}

dgn-np:NP1295040.RAg4UkZS4x4HYcGXpyVDAicwJ-imQXP9rV11ztkwPpH4c130_assertion {
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dgn-np:NP1295040.RAg4UkZS4x4HYcGXpyVDAicwJ-imQXP9rV11ztkwPpH4c130_provenance {
  dgn-np:NP1295040.RAg4UkZS4x4HYcGXpyVDAicwJ-imQXP9rV11ztkwPpH4c130_assertion dcterms:description
      "[Furthermore, identification of rare loss-of-function variants in genes such as PCSK9, NPC1L1, APOC3 and APOA5, which cause a markedly decreased risk of CHD and no adverse side effects, illustrates the power of translating genetic findings into novel mechanistic information and provides some optimism for the future of developing novel drugs, given the many genes associated with CHD in GWASs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
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    prov:wasDerivedFrom dgn-void:befree-2016;
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  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
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dgn-np:NP1295040.RAg4UkZS4x4HYcGXpyVDAicwJ-imQXP9rV11ztkwPpH4c130_publicationInfo {
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