@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP898818.RAJwXG1v3e3ycRhHaZx1Hcxq1kvc3LGnaVKDfSTRVFPeI> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP898818.RAJwXG1v3e3ycRhHaZx1Hcxq1kvc3LGnaVKDfSTRVFPeI130_head {
  this: np:hasAssertion dgn-np:NP898818.RAJwXG1v3e3ycRhHaZx1Hcxq1kvc3LGnaVKDfSTRVFPeI130_assertion;
    np:hasProvenance dgn-np:NP898818.RAJwXG1v3e3ycRhHaZx1Hcxq1kvc3LGnaVKDfSTRVFPeI130_provenance;
    np:hasPublicationInfo dgn-np:NP898818.RAJwXG1v3e3ycRhHaZx1Hcxq1kvc3LGnaVKDfSTRVFPeI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP898818.RAJwXG1v3e3ycRhHaZx1Hcxq1kvc3LGnaVKDfSTRVFPeI130_assertion a np:Assertion .
  
  dgn-np:NP898818.RAJwXG1v3e3ycRhHaZx1Hcxq1kvc3LGnaVKDfSTRVFPeI130_provenance a np:Provenance .
  
  dgn-np:NP898818.RAJwXG1v3e3ycRhHaZx1Hcxq1kvc3LGnaVKDfSTRVFPeI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP898818.RAJwXG1v3e3ycRhHaZx1Hcxq1kvc3LGnaVKDfSTRVFPeI130_assertion {
  miriam-gene:3172 a ncit:C16612 .
  
  lld:C0011849 a ncit:C7057 .
  
  dgn-gda:DGN0e62324472685984dfa91b9d6d477d46 sio:SIO_000628 miriam-gene:3172, lld:C0011849;
    a sio:SIO_001122 .
}

dgn-np:NP898818.RAJwXG1v3e3ycRhHaZx1Hcxq1kvc3LGnaVKDfSTRVFPeI130_provenance {
  dgn-np:NP898818.RAJwXG1v3e3ycRhHaZx1Hcxq1kvc3LGnaVKDfSTRVFPeI130_assertion dcterms:description
      "[Nine SNPs spanning the HNF4 alpha P2 promoter (rs4810424, rs1884613 and rs1884614) and coding region (rs2144908, rs6031551, rs6031552, rs1885088, rs1028583 and rs3818247) were genotyped in 160 subjects without diabetes or metabolic syndrome.]. 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:21633728;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP898818.RAJwXG1v3e3ycRhHaZx1Hcxq1kvc3LGnaVKDfSTRVFPeI130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:31+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}