@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP533555.RAwqF9ufkQKnbRr82cdZWozN7QZ2z3a0XPEku4TQDDrcA> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP533555.RAwqF9ufkQKnbRr82cdZWozN7QZ2z3a0XPEku4TQDDrcA130_head {
  this: np:hasAssertion dgn-np:NP533555.RAwqF9ufkQKnbRr82cdZWozN7QZ2z3a0XPEku4TQDDrcA130_assertion;
    np:hasProvenance dgn-np:NP533555.RAwqF9ufkQKnbRr82cdZWozN7QZ2z3a0XPEku4TQDDrcA130_provenance;
    np:hasPublicationInfo dgn-np:NP533555.RAwqF9ufkQKnbRr82cdZWozN7QZ2z3a0XPEku4TQDDrcA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP533555.RAwqF9ufkQKnbRr82cdZWozN7QZ2z3a0XPEku4TQDDrcA130_assertion a np:Assertion .
  
  dgn-np:NP533555.RAwqF9ufkQKnbRr82cdZWozN7QZ2z3a0XPEku4TQDDrcA130_provenance a np:Provenance .
  
  dgn-np:NP533555.RAwqF9ufkQKnbRr82cdZWozN7QZ2z3a0XPEku4TQDDrcA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP533555.RAwqF9ufkQKnbRr82cdZWozN7QZ2z3a0XPEku4TQDDrcA130_assertion {
  miriam-gene:3949 a ncit:C16612 .
  
  lld:C0342880 a ncit:C7057 .
  
  dgn-gda:DGN2bf4d74efaf9969c2503ba0162bb98c4 sio:SIO_000628 miriam-gene:3949, lld:C0342880;
    a sio:SIO_001121 .
}

dgn-np:NP533555.RAwqF9ufkQKnbRr82cdZWozN7QZ2z3a0XPEku4TQDDrcA130_provenance {
  dgn-np:NP533555.RAwqF9ufkQKnbRr82cdZWozN7QZ2z3a0XPEku4TQDDrcA130_assertion dcterms:description
      "[The ability to identify mutant LDL receptor genes for prenatal diagnosis of homozygous FH or to study the role of the LDL receptor gene in polygenic hypercholesterolemia requires the use of closely linked RFLPs.]. 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:2563635;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP533555.RAwqF9ufkQKnbRr82cdZWozN7QZ2z3a0XPEku4TQDDrcA130_publicationInfo {
  this: dcterms:created "2015-08-25T14:42:55+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}