@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP747670.RAUlOlvsatmNO4gc2EScKja8O_pjWbLd-4g4xmajFsR_4> .
@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:NP747670.RAUlOlvsatmNO4gc2EScKja8O_pjWbLd-4g4xmajFsR_4130_head {
  this: np:hasAssertion dgn-np:NP747670.RAUlOlvsatmNO4gc2EScKja8O_pjWbLd-4g4xmajFsR_4130_assertion;
    np:hasProvenance dgn-np:NP747670.RAUlOlvsatmNO4gc2EScKja8O_pjWbLd-4g4xmajFsR_4130_provenance;
    np:hasPublicationInfo dgn-np:NP747670.RAUlOlvsatmNO4gc2EScKja8O_pjWbLd-4g4xmajFsR_4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP747670.RAUlOlvsatmNO4gc2EScKja8O_pjWbLd-4g4xmajFsR_4130_assertion a np:Assertion .
  
  dgn-np:NP747670.RAUlOlvsatmNO4gc2EScKja8O_pjWbLd-4g4xmajFsR_4130_provenance a np:Provenance .
  
  dgn-np:NP747670.RAUlOlvsatmNO4gc2EScKja8O_pjWbLd-4g4xmajFsR_4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP747670.RAUlOlvsatmNO4gc2EScKja8O_pjWbLd-4g4xmajFsR_4130_assertion {
  miriam-gene:23564 a ncit:C16612 .
  
  lld:C0007222 a ncit:C7057 .
  
  dgn-gda:DGN0dfb508469b6590923893ca620c67f6d sio:SIO_000628 miriam-gene:23564, lld:C0007222;
    a sio:SIO_001121 .
}

dgn-np:NP747670.RAUlOlvsatmNO4gc2EScKja8O_pjWbLd-4g4xmajFsR_4130_provenance {
  dgn-np:NP747670.RAUlOlvsatmNO4gc2EScKja8O_pjWbLd-4g4xmajFsR_4130_assertion dcterms:description
      "[The discovery of a functional polymorphism within the DDAH2 promoter suggests that there may be common, individual differences in the ability to metabolise ADMA in vivo, that in turn, might underlie susceptibility to cardiovascular disease.]. 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:14550280;
    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:NP747670.RAUlOlvsatmNO4gc2EScKja8O_pjWbLd-4g4xmajFsR_4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:33+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" .
}