@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP861515.RAR6AmUlEs0MUdOw1Vt8gyDT0FgNkiwVYbxzIcUwjCv2g> .
@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:NP861515.RAR6AmUlEs0MUdOw1Vt8gyDT0FgNkiwVYbxzIcUwjCv2g130_head {
  this: np:hasAssertion dgn-np:NP861515.RAR6AmUlEs0MUdOw1Vt8gyDT0FgNkiwVYbxzIcUwjCv2g130_assertion;
    np:hasProvenance dgn-np:NP861515.RAR6AmUlEs0MUdOw1Vt8gyDT0FgNkiwVYbxzIcUwjCv2g130_provenance;
    np:hasPublicationInfo dgn-np:NP861515.RAR6AmUlEs0MUdOw1Vt8gyDT0FgNkiwVYbxzIcUwjCv2g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP861515.RAR6AmUlEs0MUdOw1Vt8gyDT0FgNkiwVYbxzIcUwjCv2g130_assertion a np:Assertion .
  
  dgn-np:NP861515.RAR6AmUlEs0MUdOw1Vt8gyDT0FgNkiwVYbxzIcUwjCv2g130_provenance a np:Provenance .
  
  dgn-np:NP861515.RAR6AmUlEs0MUdOw1Vt8gyDT0FgNkiwVYbxzIcUwjCv2g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP861515.RAR6AmUlEs0MUdOw1Vt8gyDT0FgNkiwVYbxzIcUwjCv2g130_assertion {
  miriam-gene:51440 a ncit:C16612 .
  
  lld:C0020443 a ncit:C7057 .
  
  dgn-gda:DGNe3aaab72c30324de548da00031d7bdd2 sio:SIO_000628 miriam-gene:51440, lld:C0020443;
    a sio:SIO_001121 .
}

dgn-np:NP861515.RAR6AmUlEs0MUdOw1Vt8gyDT0FgNkiwVYbxzIcUwjCv2g130_provenance {
  dgn-np:NP861515.RAR6AmUlEs0MUdOw1Vt8gyDT0FgNkiwVYbxzIcUwjCv2g130_assertion dcterms:description
      "[By means of mutant allele-specific amplification we determined that the mutation co-segregated with elevated cholesterol and LDL cholesterol in the plasma of family members with HLP IIa and HLP IIb, but not with the elevated plasma triglycerides seen in HLP IIb and HLP IV 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:10807540;
    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:NP861515.RAR6AmUlEs0MUdOw1Vt8gyDT0FgNkiwVYbxzIcUwjCv2g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:46+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" .
}