@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1381473.RAvUgdSG2er1_wJFbJMrfl1Rf3sqcH_eI3PHMxhpg0W50> .
@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:NP1381473.RAvUgdSG2er1_wJFbJMrfl1Rf3sqcH_eI3PHMxhpg0W50130_head {
  this: np:hasAssertion dgn-np:NP1381473.RAvUgdSG2er1_wJFbJMrfl1Rf3sqcH_eI3PHMxhpg0W50130_assertion;
    np:hasProvenance dgn-np:NP1381473.RAvUgdSG2er1_wJFbJMrfl1Rf3sqcH_eI3PHMxhpg0W50130_provenance;
    np:hasPublicationInfo dgn-np:NP1381473.RAvUgdSG2er1_wJFbJMrfl1Rf3sqcH_eI3PHMxhpg0W50130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1381473.RAvUgdSG2er1_wJFbJMrfl1Rf3sqcH_eI3PHMxhpg0W50130_assertion a np:Assertion .
  
  dgn-np:NP1381473.RAvUgdSG2er1_wJFbJMrfl1Rf3sqcH_eI3PHMxhpg0W50130_provenance a np:Provenance .
  
  dgn-np:NP1381473.RAvUgdSG2er1_wJFbJMrfl1Rf3sqcH_eI3PHMxhpg0W50130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1381473.RAvUgdSG2er1_wJFbJMrfl1Rf3sqcH_eI3PHMxhpg0W50130_assertion {
  miriam-gene:4023 a ncit:C16612 .
  
  lld:C0023817 a ncit:C7057 .
  
  dgn-gda:DGN2ed960a098ade5303458bbfc3eced39e sio:SIO_000628 miriam-gene:4023, lld:C0023817;
    a sio:SIO_001121 .
}

dgn-np:NP1381473.RAvUgdSG2er1_wJFbJMrfl1Rf3sqcH_eI3PHMxhpg0W50130_provenance {
  dgn-np:NP1381473.RAvUgdSG2er1_wJFbJMrfl1Rf3sqcH_eI3PHMxhpg0W50130_assertion dcterms:description
      "[Patients with mutations on both alleles of the lipoprotein lipase gene resulting in complete lipoprotein lipase deficiency exhibit the chylomicronemia syndrome with severe hypertriglyceridemia and increased risk of pancreatitis and possibly of ischemic heart disease.]. 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:9323055;
    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:NP1381473.RAvUgdSG2er1_wJFbJMrfl1Rf3sqcH_eI3PHMxhpg0W50130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:12+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" .
}