@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP361381.RAsq8MVtVLEqcXnV4HpSbQ7H38G7ZZAkj5ahd66X_RqRQ> .
@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/v4.0.0/void/> .

dgn-np:NP361381.RAsq8MVtVLEqcXnV4HpSbQ7H38G7ZZAkj5ahd66X_RqRQ130_head {
  this: np:hasAssertion dgn-np:NP361381.RAsq8MVtVLEqcXnV4HpSbQ7H38G7ZZAkj5ahd66X_RqRQ130_assertion;
    np:hasProvenance dgn-np:NP361381.RAsq8MVtVLEqcXnV4HpSbQ7H38G7ZZAkj5ahd66X_RqRQ130_provenance;
    np:hasPublicationInfo dgn-np:NP361381.RAsq8MVtVLEqcXnV4HpSbQ7H38G7ZZAkj5ahd66X_RqRQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP361381.RAsq8MVtVLEqcXnV4HpSbQ7H38G7ZZAkj5ahd66X_RqRQ130_assertion a np:Assertion .
  
  dgn-np:NP361381.RAsq8MVtVLEqcXnV4HpSbQ7H38G7ZZAkj5ahd66X_RqRQ130_provenance a np:Provenance .
  
  dgn-np:NP361381.RAsq8MVtVLEqcXnV4HpSbQ7H38G7ZZAkj5ahd66X_RqRQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP361381.RAsq8MVtVLEqcXnV4HpSbQ7H38G7ZZAkj5ahd66X_RqRQ130_assertion {
  miriam-gene:3949 a ncit:C16612 .
  
  lld:C0010068 a ncit:C7057 .
  
  dgn-gda:DGN0c7983877b9ff21f1bd155160a1d53b1 sio:SIO_000628 miriam-gene:3949, lld:C0010068;
    a sio:SIO_001121 .
}

dgn-np:NP361381.RAsq8MVtVLEqcXnV4HpSbQ7H38G7ZZAkj5ahd66X_RqRQ130_provenance {
  dgn-np:NP361381.RAsq8MVtVLEqcXnV4HpSbQ7H38G7ZZAkj5ahd66X_RqRQ130_assertion dcterms:description
      "[This disease, which is due to mutation in the low density lipoprotein (LDL) receptor gene and results in deficiency of the LDL receptor, is associated with hypercholesterolemia and premature development of coronary heart disease.]. 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:12119548;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP361381.RAsq8MVtVLEqcXnV4HpSbQ7H38G7ZZAkj5ahd66X_RqRQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:29+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}