@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP190111.RAYWt1qc54q8XO0yvoAu4uT6H9tuk3XwMP9Z0bqLd1PIg> .
@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:NP190111.RAYWt1qc54q8XO0yvoAu4uT6H9tuk3XwMP9Z0bqLd1PIg130_head {
  this: np:hasAssertion dgn-np:NP190111.RAYWt1qc54q8XO0yvoAu4uT6H9tuk3XwMP9Z0bqLd1PIg130_assertion ;
    np:hasProvenance dgn-np:NP190111.RAYWt1qc54q8XO0yvoAu4uT6H9tuk3XwMP9Z0bqLd1PIg130_provenance ;
    np:hasPublicationInfo dgn-np:NP190111.RAYWt1qc54q8XO0yvoAu4uT6H9tuk3XwMP9Z0bqLd1PIg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP190111.RAYWt1qc54q8XO0yvoAu4uT6H9tuk3XwMP9Z0bqLd1PIg130_assertion a np:Assertion .
  dgn-np:NP190111.RAYWt1qc54q8XO0yvoAu4uT6H9tuk3XwMP9Z0bqLd1PIg130_provenance a np:Provenance .
  dgn-np:NP190111.RAYWt1qc54q8XO0yvoAu4uT6H9tuk3XwMP9Z0bqLd1PIg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP190111.RAYWt1qc54q8XO0yvoAu4uT6H9tuk3XwMP9Z0bqLd1PIg130_assertion {
  miriam-gene:404677 a ncit:C16612 .
  lld:C0020538 a ncit:C7057 .
  dgn-gda:DGN64f73beed4480a9fab88a7705db9787b sio:SIO_000628 miriam-gene:404677 , lld:C0020538 ;
    a sio:SIO_001121 .
}
dgn-np:NP190111.RAYWt1qc54q8XO0yvoAu4uT6H9tuk3XwMP9Z0bqLd1PIg130_provenance {
  dgn-np:NP190111.RAYWt1qc54q8XO0yvoAu4uT6H9tuk3XwMP9Z0bqLd1PIg130_assertion dcterms:description "[While there is no evidence for a significant association of several common lipoprotein-related genetic variants with carotid IMT, our results are consistent with the previously reported role of CETP and LPL genetic variants in cardiovascular risk and the possible modulation of the association between hypertension and carotid IMT by APOCIII Sst-1 variant.]. 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:16430904 ;
    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:NP190111.RAYWt1qc54q8XO0yvoAu4uT6H9tuk3XwMP9Z0bqLd1PIg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:44+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" .
}