@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP688130.RATNuDwFXMS2zJIn1UaRBeyUVdhQB52QvG0mpCo5dinnU> .
@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:NP688130.RATNuDwFXMS2zJIn1UaRBeyUVdhQB52QvG0mpCo5dinnU130_head {
  this: np:hasAssertion dgn-np:NP688130.RATNuDwFXMS2zJIn1UaRBeyUVdhQB52QvG0mpCo5dinnU130_assertion;
    np:hasProvenance dgn-np:NP688130.RATNuDwFXMS2zJIn1UaRBeyUVdhQB52QvG0mpCo5dinnU130_provenance;
    np:hasPublicationInfo dgn-np:NP688130.RATNuDwFXMS2zJIn1UaRBeyUVdhQB52QvG0mpCo5dinnU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP688130.RATNuDwFXMS2zJIn1UaRBeyUVdhQB52QvG0mpCo5dinnU130_assertion a np:Assertion .
  
  dgn-np:NP688130.RATNuDwFXMS2zJIn1UaRBeyUVdhQB52QvG0mpCo5dinnU130_provenance a np:Provenance .
  
  dgn-np:NP688130.RATNuDwFXMS2zJIn1UaRBeyUVdhQB52QvG0mpCo5dinnU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP688130.RATNuDwFXMS2zJIn1UaRBeyUVdhQB52QvG0mpCo5dinnU130_assertion {
  miriam-gene:217 a ncit:C16612 .
  
  lld:C0010068 a ncit:C7057 .
  
  dgn-gda:DGNab00b8a8b3b2c31ce25806b23908fdac sio:SIO_000628 miriam-gene:217, lld:C0010068;
    a sio:SIO_001121 .
}

dgn-np:NP688130.RATNuDwFXMS2zJIn1UaRBeyUVdhQB52QvG0mpCo5dinnU130_provenance {
  dgn-np:NP688130.RATNuDwFXMS2zJIn1UaRBeyUVdhQB52QvG0mpCo5dinnU130_assertion dcterms:description
      "[These findings suggest that the ALDH2 polymorphism is associated with an increased risk of T2DM in female CAD patients, and this association could be causal on the basis of the association between the polymorphism and FPG, which is partly explained by an increased inflammatory status.]. 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:19876063;
    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:NP688130.RATNuDwFXMS2zJIn1UaRBeyUVdhQB52QvG0mpCo5dinnU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:58+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" .
}