@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP587366.RANhfXaGz07_fizHdS2CXT3J42ZzFQw5EvpIMLHIlectQ> .
@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:NP587366.RANhfXaGz07_fizHdS2CXT3J42ZzFQw5EvpIMLHIlectQ130_head {
  this: np:hasAssertion dgn-np:NP587366.RANhfXaGz07_fizHdS2CXT3J42ZzFQw5EvpIMLHIlectQ130_assertion ;
    np:hasProvenance dgn-np:NP587366.RANhfXaGz07_fizHdS2CXT3J42ZzFQw5EvpIMLHIlectQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP587366.RANhfXaGz07_fizHdS2CXT3J42ZzFQw5EvpIMLHIlectQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP587366.RANhfXaGz07_fizHdS2CXT3J42ZzFQw5EvpIMLHIlectQ130_assertion a np:Assertion .
  dgn-np:NP587366.RANhfXaGz07_fizHdS2CXT3J42ZzFQw5EvpIMLHIlectQ130_provenance a np:Provenance .
  dgn-np:NP587366.RANhfXaGz07_fizHdS2CXT3J42ZzFQw5EvpIMLHIlectQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP587366.RANhfXaGz07_fizHdS2CXT3J42ZzFQw5EvpIMLHIlectQ130_assertion {
  miriam-gene:6363 a ncit:C16612 .
  lld:C0004153 a ncit:C7057 .
  dgn-gda:DGN0009cb9cd9d7eb6fc52add88e3a979ef sio:SIO_000628 miriam-gene:6363 , lld:C0004153 ;
    a sio:SIO_001121 .
}
dgn-np:NP587366.RANhfXaGz07_fizHdS2CXT3J42ZzFQw5EvpIMLHIlectQ130_provenance {
  dgn-np:NP587366.RANhfXaGz07_fizHdS2CXT3J42ZzFQw5EvpIMLHIlectQ130_assertion dcterms:description "[The mean terminal restriction fragment (TRF) was determined by Southern blot hybridization in the peripheral blood cells of 34 male Japanese patients with metabolic syndrome (MetS) who were under 70 years of age with (n=17) and without (n=17) bilateral ELC, and assessed the relationship of ELC to atherosclerotic cardiovascular disease (AVD).]. 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:19060421 ;
    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:NP587366.RANhfXaGz07_fizHdS2CXT3J42ZzFQw5EvpIMLHIlectQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:53+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> ;
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}