@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP618290.RAFJT16MVj9KIYSR2YkGzV0C1BI2m8kPIleVOVKf9IXNc> .
@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:NP618290.RAFJT16MVj9KIYSR2YkGzV0C1BI2m8kPIleVOVKf9IXNc130_head {
  this: np:hasAssertion dgn-np:NP618290.RAFJT16MVj9KIYSR2YkGzV0C1BI2m8kPIleVOVKf9IXNc130_assertion;
    np:hasProvenance dgn-np:NP618290.RAFJT16MVj9KIYSR2YkGzV0C1BI2m8kPIleVOVKf9IXNc130_provenance;
    np:hasPublicationInfo dgn-np:NP618290.RAFJT16MVj9KIYSR2YkGzV0C1BI2m8kPIleVOVKf9IXNc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP618290.RAFJT16MVj9KIYSR2YkGzV0C1BI2m8kPIleVOVKf9IXNc130_assertion a np:Assertion .
  
  dgn-np:NP618290.RAFJT16MVj9KIYSR2YkGzV0C1BI2m8kPIleVOVKf9IXNc130_provenance a np:Provenance .
  
  dgn-np:NP618290.RAFJT16MVj9KIYSR2YkGzV0C1BI2m8kPIleVOVKf9IXNc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP618290.RAFJT16MVj9KIYSR2YkGzV0C1BI2m8kPIleVOVKf9IXNc130_assertion {
  miriam-gene:335 a ncit:C16612 .
  
  lld:C0020474 a ncit:C7057 .
  
  dgn-gda:DGNb64ebfd10fb6cde69a73410bbab846b0 sio:SIO_000628 miriam-gene:335, lld:C0020474;
    a sio:SIO_001121 .
}

dgn-np:NP618290.RAFJT16MVj9KIYSR2YkGzV0C1BI2m8kPIleVOVKf9IXNc130_provenance {
  dgn-np:NP618290.RAFJT16MVj9KIYSR2YkGzV0C1BI2m8kPIleVOVKf9IXNc130_assertion dcterms:description
      "[By using chemical cleavage mismatch analysis and the single strand conformation polymorphism technique, DNA fragments of the apo CIII gene, including the 5' flanking region and all the exons, were screened for sequence changes underlying the observed association between familial combined hyperlipidaemia (FCHL) and the apo AI-CIII-AIV gene cluster in affected individuals from eight FCHL families.]. 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:7889654;
    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:NP618290.RAFJT16MVj9KIYSR2YkGzV0C1BI2m8kPIleVOVKf9IXNc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:13+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" .
}