@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP244935.RAb-fJrqr0siYd3ldIvmPd1C9s5wmZIb4hqcJaq45Jn5Y> .
@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:NP244935.RAb-fJrqr0siYd3ldIvmPd1C9s5wmZIb4hqcJaq45Jn5Y130_head {
  this: np:hasAssertion dgn-np:NP244935.RAb-fJrqr0siYd3ldIvmPd1C9s5wmZIb4hqcJaq45Jn5Y130_assertion;
    np:hasProvenance dgn-np:NP244935.RAb-fJrqr0siYd3ldIvmPd1C9s5wmZIb4hqcJaq45Jn5Y130_provenance;
    np:hasPublicationInfo dgn-np:NP244935.RAb-fJrqr0siYd3ldIvmPd1C9s5wmZIb4hqcJaq45Jn5Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP244935.RAb-fJrqr0siYd3ldIvmPd1C9s5wmZIb4hqcJaq45Jn5Y130_assertion a np:Assertion .
  
  dgn-np:NP244935.RAb-fJrqr0siYd3ldIvmPd1C9s5wmZIb4hqcJaq45Jn5Y130_provenance a np:Provenance .
  
  dgn-np:NP244935.RAb-fJrqr0siYd3ldIvmPd1C9s5wmZIb4hqcJaq45Jn5Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP244935.RAb-fJrqr0siYd3ldIvmPd1C9s5wmZIb4hqcJaq45Jn5Y130_assertion {
  miriam-gene:7391 a ncit:C16612 .
  
  lld:C0020473 a ncit:C7057 .
  
  dgn-gda:DGNac0c125314db220b02f64abe271dc52f sio:SIO_000628 miriam-gene:7391, lld:C0020473;
    a sio:SIO_001121 .
}

dgn-np:NP244935.RAb-fJrqr0siYd3ldIvmPd1C9s5wmZIb4hqcJaq45Jn5Y130_provenance {
  dgn-np:NP244935.RAb-fJrqr0siYd3ldIvmPd1C9s5wmZIb4hqcJaq45Jn5Y130_assertion dcterms:description
      "[The genetic defect of familial combined hyperlipidemia (FCHL) is still unknown although FCHL is speculated to be the most prevalent genetic hyperlipidemia, and further investigations should be performed to elucidate the molecular mechanisms of FCHL]. 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:15256764;
    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:NP244935.RAb-fJrqr0siYd3ldIvmPd1C9s5wmZIb4hqcJaq45Jn5Y130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:17+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" .
}