@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1259625.RAM16rq02v0kqzdzemXbJailoreyTb7hEgcFxY6fvt0F4> .
@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:NP1259625.RAM16rq02v0kqzdzemXbJailoreyTb7hEgcFxY6fvt0F4130_head {
  this: np:hasAssertion dgn-np:NP1259625.RAM16rq02v0kqzdzemXbJailoreyTb7hEgcFxY6fvt0F4130_assertion ;
    np:hasProvenance dgn-np:NP1259625.RAM16rq02v0kqzdzemXbJailoreyTb7hEgcFxY6fvt0F4130_provenance ;
    np:hasPublicationInfo dgn-np:NP1259625.RAM16rq02v0kqzdzemXbJailoreyTb7hEgcFxY6fvt0F4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1259625.RAM16rq02v0kqzdzemXbJailoreyTb7hEgcFxY6fvt0F4130_assertion a np:Assertion .
  dgn-np:NP1259625.RAM16rq02v0kqzdzemXbJailoreyTb7hEgcFxY6fvt0F4130_provenance a np:Provenance .
  dgn-np:NP1259625.RAM16rq02v0kqzdzemXbJailoreyTb7hEgcFxY6fvt0F4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1259625.RAM16rq02v0kqzdzemXbJailoreyTb7hEgcFxY6fvt0F4130_assertion {
  miriam-gene:3949 a ncit:C16612 .
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    a sio:SIO_001121 .
}
dgn-np:NP1259625.RAM16rq02v0kqzdzemXbJailoreyTb7hEgcFxY6fvt0F4130_provenance {
  dgn-np:NP1259625.RAM16rq02v0kqzdzemXbJailoreyTb7hEgcFxY6fvt0F4130_assertion dcterms:description "[The ability to identify mutant LDL receptor genes for prenatal diagnosis of homozygous FH or to study the role of the LDL receptor gene in polygenic hypercholesterolemia requires the use of closely linked RFLPs.]. 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:2563635 ;
    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:NP1259625.RAM16rq02v0kqzdzemXbJailoreyTb7hEgcFxY6fvt0F4130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:17+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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    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" .
}