@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP711923.RAM6QvfGLtbkzXtf9UUc-itziabMVg6CLlrJkmjM8Dank> .
@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:NP711923.RAM6QvfGLtbkzXtf9UUc-itziabMVg6CLlrJkmjM8Dank130_head {
   this: np:hasAssertion dgn-np:NP711923.RAM6QvfGLtbkzXtf9UUc-itziabMVg6CLlrJkmjM8Dank130_assertion ;
    np:hasProvenance dgn-np:NP711923.RAM6QvfGLtbkzXtf9UUc-itziabMVg6CLlrJkmjM8Dank130_provenance ;
    np:hasPublicationInfo dgn-np:NP711923.RAM6QvfGLtbkzXtf9UUc-itziabMVg6CLlrJkmjM8Dank130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP711923.RAM6QvfGLtbkzXtf9UUc-itziabMVg6CLlrJkmjM8Dank130_assertion a np:Assertion .
  dgn-np:NP711923.RAM6QvfGLtbkzXtf9UUc-itziabMVg6CLlrJkmjM8Dank130_provenance a np:Provenance .
  dgn-np:NP711923.RAM6QvfGLtbkzXtf9UUc-itziabMVg6CLlrJkmjM8Dank130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP711923.RAM6QvfGLtbkzXtf9UUc-itziabMVg6CLlrJkmjM8Dank130_assertion {
   miriam-gene:4953 a ncit:C16612 .
  lld:C0017154 a ncit:C7057 .
  dgn-gda:DGN1e6c2abffdaf18d34a39f675f61dfdbe sio:SIO_000628 miriam-gene:4953 , lld:C0017154 ;
    a sio:SIO_001121 .
}
dgn-np:NP711923.RAM6QvfGLtbkzXtf9UUc-itziabMVg6CLlrJkmjM8Dank130_provenance {
   dgn-np:NP711923.RAM6QvfGLtbkzXtf9UUc-itziabMVg6CLlrJkmjM8Dank130_assertion dcterms:description "[In subjects with mild chronic atrophic gastritis, the frequencies of the variant (less common) alleles of CYP2E1 RsaI, CYP2E1 DraI, GSTP1, ALDH2, and ODC were, respectively, 0.156, 0.201, 0.189, 0.190, and 0.428.]. 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:15734972 ;
    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:NP711923.RAM6QvfGLtbkzXtf9UUc-itziabMVg6CLlrJkmjM8Dank130_publicationInfo {
   this: dcterms:created "2014-10-02T12:39:12+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" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}