@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP746108.RADEd8QCOP6OUPH10n41arnMUe2mhDzWsyjNbu2YXGx6Y> .
@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:NP746108.RADEd8QCOP6OUPH10n41arnMUe2mhDzWsyjNbu2YXGx6Y130_head {
  this: np:hasAssertion dgn-np:NP746108.RADEd8QCOP6OUPH10n41arnMUe2mhDzWsyjNbu2YXGx6Y130_assertion ;
    np:hasProvenance dgn-np:NP746108.RADEd8QCOP6OUPH10n41arnMUe2mhDzWsyjNbu2YXGx6Y130_provenance ;
    np:hasPublicationInfo dgn-np:NP746108.RADEd8QCOP6OUPH10n41arnMUe2mhDzWsyjNbu2YXGx6Y130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP746108.RADEd8QCOP6OUPH10n41arnMUe2mhDzWsyjNbu2YXGx6Y130_assertion a np:Assertion .
  dgn-np:NP746108.RADEd8QCOP6OUPH10n41arnMUe2mhDzWsyjNbu2YXGx6Y130_provenance a np:Provenance .
  dgn-np:NP746108.RADEd8QCOP6OUPH10n41arnMUe2mhDzWsyjNbu2YXGx6Y130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP746108.RADEd8QCOP6OUPH10n41arnMUe2mhDzWsyjNbu2YXGx6Y130_assertion {
  miriam-gene:255738 a ncit:C16612 .
  lld:C0020445 a ncit:C7057 .
  dgn-gda:DGN98cbd0a62c1c8036c0b23e97b6156aed sio:SIO_000628 miriam-gene:255738 , lld:C0020445 ;
    a sio:SIO_001121 .
}
dgn-np:NP746108.RADEd8QCOP6OUPH10n41arnMUe2mhDzWsyjNbu2YXGx6Y130_provenance {
  dgn-np:NP746108.RADEd8QCOP6OUPH10n41arnMUe2mhDzWsyjNbu2YXGx6Y130_assertion dcterms:description "[We present data from a cohort of 611 patients referred with suspected heterozygous familial hypercholesterolaemia (FH) from five UK lipid clinics, who were initially screened for point mutations in LDLR and the common APOB and PCSK9 mutations.]. 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:19538517 ;
    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:NP746108.RADEd8QCOP6OUPH10n41arnMUe2mhDzWsyjNbu2YXGx6Y130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:23+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" .
}