@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP63696.RATF2op6T3EwfgVg-syzAWTgRUEm4cIxFVw488whQfIYk> .
@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:NP63696.RATF2op6T3EwfgVg-syzAWTgRUEm4cIxFVw488whQfIYk130_head {
  this: np:hasAssertion dgn-np:NP63696.RATF2op6T3EwfgVg-syzAWTgRUEm4cIxFVw488whQfIYk130_assertion;
    np:hasProvenance dgn-np:NP63696.RATF2op6T3EwfgVg-syzAWTgRUEm4cIxFVw488whQfIYk130_provenance;
    np:hasPublicationInfo dgn-np:NP63696.RATF2op6T3EwfgVg-syzAWTgRUEm4cIxFVw488whQfIYk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP63696.RATF2op6T3EwfgVg-syzAWTgRUEm4cIxFVw488whQfIYk130_assertion a np:Assertion .
  
  dgn-np:NP63696.RATF2op6T3EwfgVg-syzAWTgRUEm4cIxFVw488whQfIYk130_provenance a np:Provenance .
  
  dgn-np:NP63696.RATF2op6T3EwfgVg-syzAWTgRUEm4cIxFVw488whQfIYk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP63696.RATF2op6T3EwfgVg-syzAWTgRUEm4cIxFVw488whQfIYk130_assertion {
  miriam-gene:55937 a ncit:C16612 .
  
  lld:C0011860 a ncit:C7057 .
  
  dgn-gda:DGN003ce28dd73ff825b2883213fde6fc33 sio:SIO_000628 miriam-gene:55937, lld:C0011860;
    a sio:SIO_001122 .
}

dgn-np:NP63696.RATF2op6T3EwfgVg-syzAWTgRUEm4cIxFVw488whQfIYk130_provenance {
  dgn-np:NP63696.RATF2op6T3EwfgVg-syzAWTgRUEm4cIxFVw488whQfIYk130_assertion dcterms:description
      "[The present study provided the first evidence that SNP T-778C in the proximal promoter region of apoM gene was associated with the levels of plasma CHO and FPG and also conferred the risk in the development of T2D among Han Chinese.]. 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:16572495;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP63696.RATF2op6T3EwfgVg-syzAWTgRUEm4cIxFVw488whQfIYk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:30+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" .
}