@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP796369.RAiZeOEe4CJml-_fXV9ZH5KEeajWeqoIIUWVN5aKvPgM4> .
@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:NP796369.RAiZeOEe4CJml-_fXV9ZH5KEeajWeqoIIUWVN5aKvPgM4130_head {
  this: np:hasAssertion dgn-np:NP796369.RAiZeOEe4CJml-_fXV9ZH5KEeajWeqoIIUWVN5aKvPgM4130_assertion ;
    np:hasProvenance dgn-np:NP796369.RAiZeOEe4CJml-_fXV9ZH5KEeajWeqoIIUWVN5aKvPgM4130_provenance ;
    np:hasPublicationInfo dgn-np:NP796369.RAiZeOEe4CJml-_fXV9ZH5KEeajWeqoIIUWVN5aKvPgM4130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP796369.RAiZeOEe4CJml-_fXV9ZH5KEeajWeqoIIUWVN5aKvPgM4130_provenance a np:Provenance .
  dgn-np:NP796369.RAiZeOEe4CJml-_fXV9ZH5KEeajWeqoIIUWVN5aKvPgM4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP796369.RAiZeOEe4CJml-_fXV9ZH5KEeajWeqoIIUWVN5aKvPgM4130_assertion {
  miriam-gene:4552 a ncit:C16612 .
  lld:C0024117 a ncit:C7057 .
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    a sio:SIO_001121 .
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dgn-np:NP796369.RAiZeOEe4CJml-_fXV9ZH5KEeajWeqoIIUWVN5aKvPgM4130_provenance {
  dgn-np:NP796369.RAiZeOEe4CJml-_fXV9ZH5KEeajWeqoIIUWVN5aKvPgM4130_assertion dcterms:description "[At the multiple logistic regression analysis adjusted for traditional cardiovascular risk factors (sex, age, hypertension, smoking habit, dyslipidaemia, diabetes) and chronic obstructive pulmonary disease (COPD), rs8003379 MTHFD1 (odds ratio (OR) 0.41, 95% confidence interval (CI) 0.26 to 0.65) and rs326118 MTRR (OR 0.47, 95% CI 0.29 to 0.77) polymorphisms resulted in independent susceptibility factor for AAA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP796369.RAiZeOEe4CJml-_fXV9ZH5KEeajWeqoIIUWVN5aKvPgM4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:09+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
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