@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP222397.RAO19kFHnROFJYTvoQmk0JGHPD9maHsgACUKNsO6DXgmU> .
@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:NP222397.RAO19kFHnROFJYTvoQmk0JGHPD9maHsgACUKNsO6DXgmU130_head {
  this: np:hasAssertion dgn-np:NP222397.RAO19kFHnROFJYTvoQmk0JGHPD9maHsgACUKNsO6DXgmU130_assertion ;
    np:hasProvenance dgn-np:NP222397.RAO19kFHnROFJYTvoQmk0JGHPD9maHsgACUKNsO6DXgmU130_provenance ;
    np:hasPublicationInfo dgn-np:NP222397.RAO19kFHnROFJYTvoQmk0JGHPD9maHsgACUKNsO6DXgmU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP222397.RAO19kFHnROFJYTvoQmk0JGHPD9maHsgACUKNsO6DXgmU130_assertion a np:Assertion .
  dgn-np:NP222397.RAO19kFHnROFJYTvoQmk0JGHPD9maHsgACUKNsO6DXgmU130_provenance a np:Provenance .
  dgn-np:NP222397.RAO19kFHnROFJYTvoQmk0JGHPD9maHsgACUKNsO6DXgmU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP222397.RAO19kFHnROFJYTvoQmk0JGHPD9maHsgACUKNsO6DXgmU130_assertion {
  miriam-gene:3949 a ncit:C16612 .
  lld:C0242339 a ncit:C7057 .
  dgn-gda:DGNab8754c7181c82a90c1db2b4ae699b04 sio:SIO_000628 miriam-gene:3949 , lld:C0242339 ;
    a sio:SIO_001121 .
}
dgn-np:NP222397.RAO19kFHnROFJYTvoQmk0JGHPD9maHsgACUKNsO6DXgmU130_provenance {
  dgn-np:NP222397.RAO19kFHnROFJYTvoQmk0JGHPD9maHsgACUKNsO6DXgmU130_assertion dcterms:description "[Common familial lipid disorders associated with premature heart disease include familial lipoprotein(a) excess, familial dyslipidemia (elevated triglycerides and decreased HDL cholesterol), familial combined hyperlipidemia (elevations of LDL cholesterol and triglycerides, and often decreased HDL cholesterol), familial hypoapobetalipoproteinemia (elevated apolipoprotein B levels), familial hypoalphalipoproteinemia (low HDL cholesterol levels), and familial hypercholesterolemia (elevated LDL cholesterol levels).]. 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:7802728 ;
    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:NP222397.RAO19kFHnROFJYTvoQmk0JGHPD9maHsgACUKNsO6DXgmU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:03+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> ;
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    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}