@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP361382.RAYdB1xf2lDqpJC4rj_gRwibZC5dc4ykIakX70vlonsHY> .
@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:NP361382.RAYdB1xf2lDqpJC4rj_gRwibZC5dc4ykIakX70vlonsHY130_head {
  this: np:hasAssertion dgn-np:NP361382.RAYdB1xf2lDqpJC4rj_gRwibZC5dc4ykIakX70vlonsHY130_assertion;
    np:hasProvenance dgn-np:NP361382.RAYdB1xf2lDqpJC4rj_gRwibZC5dc4ykIakX70vlonsHY130_provenance;
    np:hasPublicationInfo dgn-np:NP361382.RAYdB1xf2lDqpJC4rj_gRwibZC5dc4ykIakX70vlonsHY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP361382.RAYdB1xf2lDqpJC4rj_gRwibZC5dc4ykIakX70vlonsHY130_assertion a np:Assertion .
  
  dgn-np:NP361382.RAYdB1xf2lDqpJC4rj_gRwibZC5dc4ykIakX70vlonsHY130_provenance a np:Provenance .
  
  dgn-np:NP361382.RAYdB1xf2lDqpJC4rj_gRwibZC5dc4ykIakX70vlonsHY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP361382.RAYdB1xf2lDqpJC4rj_gRwibZC5dc4ykIakX70vlonsHY130_assertion {
  miriam-gene:3949 a ncit:C16612 .
  
  lld:C0020443 a ncit:C7057 .
  
  dgn-gda:DGN456cdacd89ec3f4f5d9163641f262194 sio:SIO_000628 miriam-gene:3949, lld:C0020443;
    a sio:SIO_001121 .
}

dgn-np:NP361382.RAYdB1xf2lDqpJC4rj_gRwibZC5dc4ykIakX70vlonsHY130_provenance {
  dgn-np:NP361382.RAYdB1xf2lDqpJC4rj_gRwibZC5dc4ykIakX70vlonsHY130_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:NP361382.RAYdB1xf2lDqpJC4rj_gRwibZC5dc4ykIakX70vlonsHY130_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" .
}