@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP530544.RAFb8NRzLIjx6pxWtykJZzdcNt7fthHUt64y2q7dJ5rK8> .
@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:NP530544.RAFb8NRzLIjx6pxWtykJZzdcNt7fthHUt64y2q7dJ5rK8130_head {
  this: np:hasAssertion dgn-np:NP530544.RAFb8NRzLIjx6pxWtykJZzdcNt7fthHUt64y2q7dJ5rK8130_assertion;
    np:hasProvenance dgn-np:NP530544.RAFb8NRzLIjx6pxWtykJZzdcNt7fthHUt64y2q7dJ5rK8130_provenance;
    np:hasPublicationInfo dgn-np:NP530544.RAFb8NRzLIjx6pxWtykJZzdcNt7fthHUt64y2q7dJ5rK8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP530544.RAFb8NRzLIjx6pxWtykJZzdcNt7fthHUt64y2q7dJ5rK8130_assertion a np:Assertion .
  
  dgn-np:NP530544.RAFb8NRzLIjx6pxWtykJZzdcNt7fthHUt64y2q7dJ5rK8130_provenance a np:Provenance .
  
  dgn-np:NP530544.RAFb8NRzLIjx6pxWtykJZzdcNt7fthHUt64y2q7dJ5rK8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP530544.RAFb8NRzLIjx6pxWtykJZzdcNt7fthHUt64y2q7dJ5rK8130_assertion {
  miriam-gene:4846 a ncit:C16612 .
  
  lld:C0338656 a ncit:C7057 .
  
  dgn-gda:DGN0dd17f67243613b2e8cb31c825d7bacf sio:SIO_000628 miriam-gene:4846, lld:C0338656;
    a sio:SIO_001121 .
}

dgn-np:NP530544.RAFb8NRzLIjx6pxWtykJZzdcNt7fthHUt64y2q7dJ5rK8130_provenance {
  dgn-np:NP530544.RAFb8NRzLIjx6pxWtykJZzdcNt7fthHUt64y2q7dJ5rK8130_assertion dcterms:description
      "[In particular, the presence of eNOS TT894 genotype in patients with cognitive decline resulted significantly associated with increased plasma Hcy levels when compared with controls having the same genotype or patients having other eNOS genotypes (P = 0.02).]. 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:21607713;
    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:NP530544.RAFb8NRzLIjx6pxWtykJZzdcNt7fthHUt64y2q7dJ5rK8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:20+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" .
}