@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP52900.RATNAIuqZsxLArma1yOPepEoIxJNKsZgCoB8CgSn8oXz4> .
@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:NP52900.RATNAIuqZsxLArma1yOPepEoIxJNKsZgCoB8CgSn8oXz4130_head {
  this: np:hasAssertion dgn-np:NP52900.RATNAIuqZsxLArma1yOPepEoIxJNKsZgCoB8CgSn8oXz4130_assertion;
    np:hasProvenance dgn-np:NP52900.RATNAIuqZsxLArma1yOPepEoIxJNKsZgCoB8CgSn8oXz4130_provenance;
    np:hasPublicationInfo dgn-np:NP52900.RATNAIuqZsxLArma1yOPepEoIxJNKsZgCoB8CgSn8oXz4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP52900.RATNAIuqZsxLArma1yOPepEoIxJNKsZgCoB8CgSn8oXz4130_assertion a np:Assertion .
  
  dgn-np:NP52900.RATNAIuqZsxLArma1yOPepEoIxJNKsZgCoB8CgSn8oXz4130_provenance a np:Provenance .
  
  dgn-np:NP52900.RATNAIuqZsxLArma1yOPepEoIxJNKsZgCoB8CgSn8oXz4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP52900.RATNAIuqZsxLArma1yOPepEoIxJNKsZgCoB8CgSn8oXz4130_assertion {
  miriam-gene:5445 a ncit:C16612 .
  
  lld:C0007222 a ncit:C7057 .
  
  dgn-gda:DGNb2db0c9c7d4b7ea2a2d96515b3413615 sio:SIO_000628 miriam-gene:5445, lld:C0007222;
    a sio:SIO_001122 .
}

dgn-np:NP52900.RATNAIuqZsxLArma1yOPepEoIxJNKsZgCoB8CgSn8oXz4130_provenance {
  dgn-np:NP52900.RATNAIuqZsxLArma1yOPepEoIxJNKsZgCoB8CgSn8oXz4130_assertion dcterms:description
      "[In our study we assessed the frequency and genotype distribution of the PON1 and PON2 polymorphisms in 197 patients with familial hypercholesterolemia (FH), to determine the possible association between these mutations and susceptibility for CVD.]. 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:11257265;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP52900.RATNAIuqZsxLArma1yOPepEoIxJNKsZgCoB8CgSn8oXz4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:24+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" .
}