@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP259547.RAjGah-zHLV5kVH1fVFnV_E-THS-4lrgmxR74xcsgKXjw> .
@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:NP259547.RAjGah-zHLV5kVH1fVFnV_E-THS-4lrgmxR74xcsgKXjw130_head {
  this: np:hasAssertion dgn-np:NP259547.RAjGah-zHLV5kVH1fVFnV_E-THS-4lrgmxR74xcsgKXjw130_assertion;
    np:hasProvenance dgn-np:NP259547.RAjGah-zHLV5kVH1fVFnV_E-THS-4lrgmxR74xcsgKXjw130_provenance;
    np:hasPublicationInfo dgn-np:NP259547.RAjGah-zHLV5kVH1fVFnV_E-THS-4lrgmxR74xcsgKXjw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP259547.RAjGah-zHLV5kVH1fVFnV_E-THS-4lrgmxR74xcsgKXjw130_assertion a np:Assertion .
  
  dgn-np:NP259547.RAjGah-zHLV5kVH1fVFnV_E-THS-4lrgmxR74xcsgKXjw130_provenance a np:Provenance .
  
  dgn-np:NP259547.RAjGah-zHLV5kVH1fVFnV_E-THS-4lrgmxR74xcsgKXjw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP259547.RAjGah-zHLV5kVH1fVFnV_E-THS-4lrgmxR74xcsgKXjw130_assertion {
  miriam-gene:3949 a ncit:C16612 .
  
  lld:C0242339 a ncit:C7057 .
  
  dgn-gda:DGN44e7f62e4b7c22c265fcffd7c471f37a sio:SIO_000628 miriam-gene:3949, lld:C0242339;
    a sio:SIO_001121 .
}

dgn-np:NP259547.RAjGah-zHLV5kVH1fVFnV_E-THS-4lrgmxR74xcsgKXjw130_provenance {
  dgn-np:NP259547.RAjGah-zHLV5kVH1fVFnV_E-THS-4lrgmxR74xcsgKXjw130_assertion dcterms:description
      "[By analysis of the clinical data of 696 possible FH patients, the present report shows evidence that clinical characterization is not sufficient to distinguish between patients with genetic or environmental dyslipidemia, and so molecular diagnosis is useful in clinical practice, allowing correct identification of FH patients and their relatives, and the early implementation of therapeutic measures to reduce the elevated cardiovascular risk of these patients.]. 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:20964105;
    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:NP259547.RAjGah-zHLV5kVH1fVFnV_E-THS-4lrgmxR74xcsgKXjw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:25+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" .
}