@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP929907.RA-N8WZhNEq7nPP_3VNUJIPrbZjlojpWphv--96a67GZg> .
@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:NP929907.RA-N8WZhNEq7nPP_3VNUJIPrbZjlojpWphv--96a67GZg130_head {
  this: np:hasAssertion dgn-np:NP929907.RA-N8WZhNEq7nPP_3VNUJIPrbZjlojpWphv--96a67GZg130_assertion ;
    np:hasProvenance dgn-np:NP929907.RA-N8WZhNEq7nPP_3VNUJIPrbZjlojpWphv--96a67GZg130_provenance ;
    np:hasPublicationInfo dgn-np:NP929907.RA-N8WZhNEq7nPP_3VNUJIPrbZjlojpWphv--96a67GZg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP929907.RA-N8WZhNEq7nPP_3VNUJIPrbZjlojpWphv--96a67GZg130_assertion a np:Assertion .
  dgn-np:NP929907.RA-N8WZhNEq7nPP_3VNUJIPrbZjlojpWphv--96a67GZg130_provenance a np:Provenance .
  dgn-np:NP929907.RA-N8WZhNEq7nPP_3VNUJIPrbZjlojpWphv--96a67GZg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP929907.RA-N8WZhNEq7nPP_3VNUJIPrbZjlojpWphv--96a67GZg130_assertion {
  miriam-gene:4023 a ncit:C16612 .
  lld:C0151826 a ncit:C7057 .
  dgn-gda:DGN16efda1882a43dd998a2b6bf48e587ce sio:SIO_000628 miriam-gene:4023 , lld:C0151826 ;
    a sio:SIO_001121 .
}
dgn-np:NP929907.RA-N8WZhNEq7nPP_3VNUJIPrbZjlojpWphv--96a67GZg130_provenance {
  dgn-np:NP929907.RA-N8WZhNEq7nPP_3VNUJIPrbZjlojpWphv--96a67GZg130_assertion dcterms:description "[In the present study, the association of the heterozygous forms of low-density lipoprotein receptor gene mutations causing FH as well as of LPL gene mutations causing (P207L and G188E) or not causing (D9N and N291S) complete loss of LPL activity with angiographically assessed CAD was estimated in a cohort of 412 French Canadian men aged <60 years who consecutively underwent coronary angiography for the investigation of retrosternal pain.]. 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:9708657 ;
    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:NP929907.RA-N8WZhNEq7nPP_3VNUJIPrbZjlojpWphv--96a67GZg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:30+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" .
}