@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP588528.RAlGShM5qjZpsSOhrLe_GFK-j_PiHUo0OLIkzqbdrNjYI> .
@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:NP588528.RAlGShM5qjZpsSOhrLe_GFK-j_PiHUo0OLIkzqbdrNjYI130_head {
  this: np:hasAssertion dgn-np:NP588528.RAlGShM5qjZpsSOhrLe_GFK-j_PiHUo0OLIkzqbdrNjYI130_assertion ;
    np:hasProvenance dgn-np:NP588528.RAlGShM5qjZpsSOhrLe_GFK-j_PiHUo0OLIkzqbdrNjYI130_provenance ;
    np:hasPublicationInfo dgn-np:NP588528.RAlGShM5qjZpsSOhrLe_GFK-j_PiHUo0OLIkzqbdrNjYI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP588528.RAlGShM5qjZpsSOhrLe_GFK-j_PiHUo0OLIkzqbdrNjYI130_assertion a np:Assertion .
  dgn-np:NP588528.RAlGShM5qjZpsSOhrLe_GFK-j_PiHUo0OLIkzqbdrNjYI130_provenance a np:Provenance .
  dgn-np:NP588528.RAlGShM5qjZpsSOhrLe_GFK-j_PiHUo0OLIkzqbdrNjYI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP588528.RAlGShM5qjZpsSOhrLe_GFK-j_PiHUo0OLIkzqbdrNjYI130_assertion {
  miriam-gene:270 a ncit:C16612 .
  lld:C0004153 a ncit:C7057 .
  dgn-gda:DGN25c9f19f4af2a1e75962f88bf70ac91b sio:SIO_000628 miriam-gene:270 , lld:C0004153 ;
    a sio:SIO_001121 .
}
dgn-np:NP588528.RAlGShM5qjZpsSOhrLe_GFK-j_PiHUo0OLIkzqbdrNjYI130_provenance {
  dgn-np:NP588528.RAlGShM5qjZpsSOhrLe_GFK-j_PiHUo0OLIkzqbdrNjYI130_assertion dcterms:description "[In conclusion, there were no differences between the mutant AMPD1 allele carriers and CC homozygotes regarding surrogate values for atherosclerosis, endothelial function, dimensions and ejection fraction of the heart, glucose tolerance and other well-known cardiovascular risk factors, whereas plasminogen activator inhibitor-1 activity and von Willebrand levels were lower in the mutant AMPD1 allele carriers.]. 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:17565237 ;
    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:NP588528.RAlGShM5qjZpsSOhrLe_GFK-j_PiHUo0OLIkzqbdrNjYI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:54+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" .
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}