@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP981891.RAqDbNfRCjoO488UGmvwD82xM9S4vBrPpIPYEDdCX7Jxo> .
@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:NP981891.RAqDbNfRCjoO488UGmvwD82xM9S4vBrPpIPYEDdCX7Jxo130_head {
  this: np:hasAssertion dgn-np:NP981891.RAqDbNfRCjoO488UGmvwD82xM9S4vBrPpIPYEDdCX7Jxo130_assertion ;
    np:hasProvenance dgn-np:NP981891.RAqDbNfRCjoO488UGmvwD82xM9S4vBrPpIPYEDdCX7Jxo130_provenance ;
    np:hasPublicationInfo dgn-np:NP981891.RAqDbNfRCjoO488UGmvwD82xM9S4vBrPpIPYEDdCX7Jxo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP981891.RAqDbNfRCjoO488UGmvwD82xM9S4vBrPpIPYEDdCX7Jxo130_assertion a np:Assertion .
  dgn-np:NP981891.RAqDbNfRCjoO488UGmvwD82xM9S4vBrPpIPYEDdCX7Jxo130_provenance a np:Provenance .
  dgn-np:NP981891.RAqDbNfRCjoO488UGmvwD82xM9S4vBrPpIPYEDdCX7Jxo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP981891.RAqDbNfRCjoO488UGmvwD82xM9S4vBrPpIPYEDdCX7Jxo130_assertion {
  miriam-gene:255738 a ncit:C16612 .
  lld:C0745103 a ncit:C7057 .
  dgn-gda:DGN939e7434452a93a9aacb37868eb18764 sio:SIO_000628 miriam-gene:255738 , lld:C0745103 ;
    a sio:SIO_001121 .
}
dgn-np:NP981891.RAqDbNfRCjoO488UGmvwD82xM9S4vBrPpIPYEDdCX7Jxo130_provenance {
  dgn-np:NP981891.RAqDbNfRCjoO488UGmvwD82xM9S4vBrPpIPYEDdCX7Jxo130_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-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:NP981891.RAqDbNfRCjoO488UGmvwD82xM9S4vBrPpIPYEDdCX7Jxo130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:40+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" .
}