@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP48385.RAhzX5-xDWdWB8xdvppma77QLefylQIoRjkwuduBQ9Hmo> .
@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 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:NP48385.RAhzX5-xDWdWB8xdvppma77QLefylQIoRjkwuduBQ9Hmo130_head {
  this: np:hasAssertion dgn-np:NP48385.RAhzX5-xDWdWB8xdvppma77QLefylQIoRjkwuduBQ9Hmo130_assertion ;
    np:hasProvenance dgn-np:NP48385.RAhzX5-xDWdWB8xdvppma77QLefylQIoRjkwuduBQ9Hmo130_provenance ;
    np:hasPublicationInfo dgn-np:NP48385.RAhzX5-xDWdWB8xdvppma77QLefylQIoRjkwuduBQ9Hmo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP48385.RAhzX5-xDWdWB8xdvppma77QLefylQIoRjkwuduBQ9Hmo130_assertion a np:Assertion .
  dgn-np:NP48385.RAhzX5-xDWdWB8xdvppma77QLefylQIoRjkwuduBQ9Hmo130_provenance a np:Provenance .
  dgn-np:NP48385.RAhzX5-xDWdWB8xdvppma77QLefylQIoRjkwuduBQ9Hmo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP48385.RAhzX5-xDWdWB8xdvppma77QLefylQIoRjkwuduBQ9Hmo130_assertion {
  miriam-gene:338 a ncit:C16612 .
  lld:C0010054 a ncit:C7057 .
  dgn-gda:DGN1a006053fb94cf1e14f26531c4ca3790 sio:SIO_000628 miriam-gene:338 , lld:C0010054 ;
    a sio:SIO_001122 .
}
dgn-np:NP48385.RAhzX5-xDWdWB8xdvppma77QLefylQIoRjkwuduBQ9Hmo130_provenance {
  dgn-np:NP48385.RAhzX5-xDWdWB8xdvppma77QLefylQIoRjkwuduBQ9Hmo130_assertion dct:description "[ Despite the small size of most studies and the incomplete understanding of the effects of these polymorphisms on lipid metabolism and on final clinical implications, the findings suggest that EcoRI and SpIns/Del polymorphisms significantly increase the risk of CAD and MI. Despite the rarity of the allelic variant of EcoRI polymorphism, its presence is strongly related to the occurrence of CAD/MI. Moreover, there is a high consistency between small and large studies. The results on SpIns/Del polymorphism seem the most interesting and reliable, considering both the number of subjects analysed and the consistency of the evidence of its effect on lipid levels. These results need to be confirmed by larger and appropriately powered studies.]. 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:12818419 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP48385.RAhzX5-xDWdWB8xdvppma77QLefylQIoRjkwuduBQ9Hmo130_publicationInfo {
  this: dct:created "2014-10-02T12:32:22+02:00"^^xsd:dateTime ;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dct:rightsHolder dgn-void:IBIGroup ;
    dct:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy orcid:0000-0001-5999-6269 , orcid:0000-0002-7534-7661 , orcid:0000-0002-9383-528X , orcid:0000-0003-0169-8159 , orcid:0000-0003-1244-7654 ;
    pav:createdBy orcid:0000-0003-0169-8159 ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}