@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP250584.RADOo3UzBTby7tKL3oxsNM5ZiA53tZoMaMvTp94wikj9k> .
@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:NP250584.RADOo3UzBTby7tKL3oxsNM5ZiA53tZoMaMvTp94wikj9k130_head {
  this: np:hasAssertion dgn-np:NP250584.RADOo3UzBTby7tKL3oxsNM5ZiA53tZoMaMvTp94wikj9k130_assertion;
    np:hasProvenance dgn-np:NP250584.RADOo3UzBTby7tKL3oxsNM5ZiA53tZoMaMvTp94wikj9k130_provenance;
    np:hasPublicationInfo dgn-np:NP250584.RADOo3UzBTby7tKL3oxsNM5ZiA53tZoMaMvTp94wikj9k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP250584.RADOo3UzBTby7tKL3oxsNM5ZiA53tZoMaMvTp94wikj9k130_assertion a np:Assertion .
  
  dgn-np:NP250584.RADOo3UzBTby7tKL3oxsNM5ZiA53tZoMaMvTp94wikj9k130_provenance a np:Provenance .
  
  dgn-np:NP250584.RADOo3UzBTby7tKL3oxsNM5ZiA53tZoMaMvTp94wikj9k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP250584.RADOo3UzBTby7tKL3oxsNM5ZiA53tZoMaMvTp94wikj9k130_assertion {
  miriam-gene:3949 a ncit:C16612 .
  
  lld:C0010068 a ncit:C7057 .
  
  dgn-gda:DGN95a539367dc32f7605d1d447b8abeefb sio:SIO_000628 miriam-gene:3949, lld:C0010068;
    a sio:SIO_001121 .
}

dgn-np:NP250584.RADOo3UzBTby7tKL3oxsNM5ZiA53tZoMaMvTp94wikj9k130_provenance {
  dgn-np:NP250584.RADOo3UzBTby7tKL3oxsNM5ZiA53tZoMaMvTp94wikj9k130_assertion dcterms:description
      "[The phenotypic characterization of 1769 LDLR mutation carriers (ADH-1) revealed that in both sexes independent predictors of the presence of tendon xanthomas were age, the quintiles of LDL cholesterol, the presence of coronary heart disease (CHD) and of receptor negative mutations.]. 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:23375686;
    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:NP250584.RADOo3UzBTby7tKL3oxsNM5ZiA53tZoMaMvTp94wikj9k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:20+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" .
}