@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP246944.RANj4yeTEUT_Pg3X3wl4KjcSe1slcmI5-sN7eM_NWiL5k> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP246944.RANj4yeTEUT_Pg3X3wl4KjcSe1slcmI5-sN7eM_NWiL5k130_head {
  this: np:hasAssertion dgn-np:NP246944.RANj4yeTEUT_Pg3X3wl4KjcSe1slcmI5-sN7eM_NWiL5k130_assertion ;
    np:hasProvenance dgn-np:NP246944.RANj4yeTEUT_Pg3X3wl4KjcSe1slcmI5-sN7eM_NWiL5k130_provenance ;
    np:hasPublicationInfo dgn-np:NP246944.RANj4yeTEUT_Pg3X3wl4KjcSe1slcmI5-sN7eM_NWiL5k130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP246944.RANj4yeTEUT_Pg3X3wl4KjcSe1slcmI5-sN7eM_NWiL5k130_assertion a np:Assertion .
  dgn-np:NP246944.RANj4yeTEUT_Pg3X3wl4KjcSe1slcmI5-sN7eM_NWiL5k130_provenance a np:Provenance .
  dgn-np:NP246944.RANj4yeTEUT_Pg3X3wl4KjcSe1slcmI5-sN7eM_NWiL5k130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP246944.RANj4yeTEUT_Pg3X3wl4KjcSe1slcmI5-sN7eM_NWiL5k130_assertion {
  miriam-gene:338 a ncit:C16612 .
  lld:C1956346 a ncit:C7057 .
  dgn-gda:DGN0a5cb859e32ac684ede56389952efb07 sio:SIO_000628 miriam-gene:338 , lld:C1956346 ;
    a sio:SIO_001121 .
}
dgn-np:NP246944.RANj4yeTEUT_Pg3X3wl4KjcSe1slcmI5-sN7eM_NWiL5k130_provenance {
  dgn-np:NP246944.RANj4yeTEUT_Pg3X3wl4KjcSe1slcmI5-sN7eM_NWiL5k130_assertion dcterms:description "[The surprising result that only two mutations of apoB in the receptor-binding domain (Arg 3500 Gln and Arg 3531 Cys) were associated with defective LDL binding, hypercholesterolemia, or CAD is in stark contrast with familial hypercholesterolemia, where nearly 150 mutations of the LDL receptor have been described that disrupt its function.]. 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:9254062 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP246944.RANj4yeTEUT_Pg3X3wl4KjcSe1slcmI5-sN7eM_NWiL5k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:18+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:disgenetrdf ;
    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 "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}