@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP977608.RAzyy_-USEGTO8EddJa1Gp__Fu29xWOdPgfTByEAhlcaA> .
@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:NP977608.RAzyy_-USEGTO8EddJa1Gp__Fu29xWOdPgfTByEAhlcaA130_head {
  this: np:hasAssertion dgn-np:NP977608.RAzyy_-USEGTO8EddJa1Gp__Fu29xWOdPgfTByEAhlcaA130_assertion ;
    np:hasProvenance dgn-np:NP977608.RAzyy_-USEGTO8EddJa1Gp__Fu29xWOdPgfTByEAhlcaA130_provenance ;
    np:hasPublicationInfo dgn-np:NP977608.RAzyy_-USEGTO8EddJa1Gp__Fu29xWOdPgfTByEAhlcaA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP977608.RAzyy_-USEGTO8EddJa1Gp__Fu29xWOdPgfTByEAhlcaA130_assertion a np:Assertion .
  dgn-np:NP977608.RAzyy_-USEGTO8EddJa1Gp__Fu29xWOdPgfTByEAhlcaA130_provenance a np:Provenance .
  dgn-np:NP977608.RAzyy_-USEGTO8EddJa1Gp__Fu29xWOdPgfTByEAhlcaA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP977608.RAzyy_-USEGTO8EddJa1Gp__Fu29xWOdPgfTByEAhlcaA130_assertion {
  miriam-gene:338 a ncit:C16612 .
  lld:C0745103 a ncit:C7057 .
  dgn-gda:DGN4700efff93b69aa4f07ce5d439936047 sio:SIO_000628 miriam-gene:338 , lld:C0745103 ;
    a sio:SIO_001121 .
}
dgn-np:NP977608.RAzyy_-USEGTO8EddJa1Gp__Fu29xWOdPgfTByEAhlcaA130_provenance {
  dgn-np:NP977608.RAzyy_-USEGTO8EddJa1Gp__Fu29xWOdPgfTByEAhlcaA130_assertion dcterms:description "[A large number of genetic markers, mostly single nucleotide polymorphisms (SNP) or mutations in three genes, implicated in autosomal dominant hypercholesterolemia (ADH), viz APOB (apolipoprotein B), LDLR (low density lipoprotein receptor) and PCSK9 (proprotein convertase subtilisin/kexin type-9), have been identified and characterized.]. 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:22534770 ;
    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:NP977608.RAzyy_-USEGTO8EddJa1Gp__Fu29xWOdPgfTByEAhlcaA130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:07+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" .
}