@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP154419.RAweNdACIOe1QJdm30oE1zkcQV3OttmcNBtGXYAGZdItU> .
@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:NP154419.RAweNdACIOe1QJdm30oE1zkcQV3OttmcNBtGXYAGZdItU130_head {
  this: np:hasAssertion dgn-np:NP154419.RAweNdACIOe1QJdm30oE1zkcQV3OttmcNBtGXYAGZdItU130_assertion ;
    np:hasProvenance dgn-np:NP154419.RAweNdACIOe1QJdm30oE1zkcQV3OttmcNBtGXYAGZdItU130_provenance ;
    np:hasPublicationInfo dgn-np:NP154419.RAweNdACIOe1QJdm30oE1zkcQV3OttmcNBtGXYAGZdItU130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP154419.RAweNdACIOe1QJdm30oE1zkcQV3OttmcNBtGXYAGZdItU130_provenance a np:Provenance .
  dgn-np:NP154419.RAweNdACIOe1QJdm30oE1zkcQV3OttmcNBtGXYAGZdItU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP154419.RAweNdACIOe1QJdm30oE1zkcQV3OttmcNBtGXYAGZdItU130_assertion {
  miriam-gene:3949 a ncit:C16612 .
  lld:C1956346 a ncit:C7057 .
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    a sio:SIO_001121 .
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dgn-np:NP154419.RAweNdACIOe1QJdm30oE1zkcQV3OttmcNBtGXYAGZdItU130_provenance {
  dgn-np:NP154419.RAweNdACIOe1QJdm30oE1zkcQV3OttmcNBtGXYAGZdItU130_assertion dcterms:description "[The genetic and environmental determinants of hypertension, lipid abnormalities, and coronary artery disease (CAD) have been studied for 15 years in Utah in population-based multigenerational pedigrees (2500 subjects among 98 pedigrees), twin pairs (74 monozygous and 78 dizygous), hypertensive siblings (131 sibships), siblings with CAD before age 55 (45 sibships), and anecdotally ascertained pedigrees with type II diabetes (271 subjects among 16 pedigrees), lipoprotein lipase deficiency (106 subjects in a single pedigree), and familial hypercholesterolemia (502 heterozygotes among 50 pedigrees).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
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dgn-np:NP154419.RAweNdACIOe1QJdm30oE1zkcQV3OttmcNBtGXYAGZdItU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:22+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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