@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP248282.RARlW8VQDbx1bGH9BzqAn3B8D-F7amGNWqKuvdXUr3fUU> .
@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:NP248282.RARlW8VQDbx1bGH9BzqAn3B8D-F7amGNWqKuvdXUr3fUU130_head {
  this: np:hasAssertion dgn-np:NP248282.RARlW8VQDbx1bGH9BzqAn3B8D-F7amGNWqKuvdXUr3fUU130_assertion;
    np:hasProvenance dgn-np:NP248282.RARlW8VQDbx1bGH9BzqAn3B8D-F7amGNWqKuvdXUr3fUU130_provenance;
    np:hasPublicationInfo dgn-np:NP248282.RARlW8VQDbx1bGH9BzqAn3B8D-F7amGNWqKuvdXUr3fUU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP248282.RARlW8VQDbx1bGH9BzqAn3B8D-F7amGNWqKuvdXUr3fUU130_assertion a np:Assertion .
  
  dgn-np:NP248282.RARlW8VQDbx1bGH9BzqAn3B8D-F7amGNWqKuvdXUr3fUU130_provenance a np:Provenance .
  
  dgn-np:NP248282.RARlW8VQDbx1bGH9BzqAn3B8D-F7amGNWqKuvdXUr3fUU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP248282.RARlW8VQDbx1bGH9BzqAn3B8D-F7amGNWqKuvdXUr3fUU130_assertion {
  miriam-gene:217 a ncit:C16612 .
  
  lld:C0023896 a ncit:C7057 .
  
  dgn-gda:DGNadb006e65ec9915f6a13a44cc40cd5ec sio:SIO_000628 miriam-gene:217, lld:C0023896;
    a sio:SIO_001121 .
}

dgn-np:NP248282.RARlW8VQDbx1bGH9BzqAn3B8D-F7amGNWqKuvdXUr3fUU130_provenance {
  dgn-np:NP248282.RARlW8VQDbx1bGH9BzqAn3B8D-F7amGNWqKuvdXUr3fUU130_assertion dcterms:description
      "[These results confirmed the previous observation that the incidence of ALDH2 deficiency is much lower in alcoholic liver disease patients than in the general population, and suggested that most of the ALDH2 deficient patients with alcoholic liver disease are heterozygous for the normal and mutant ALDH2 genes.]. 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:1916152;
    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:NP248282.RARlW8VQDbx1bGH9BzqAn3B8D-F7amGNWqKuvdXUr3fUU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:19+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" .
}