@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP280633.RAnezNV00tm5bSyznrT4uA29iFgM69eOLuysUhcafKWEs> .
@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:NP280633.RAnezNV00tm5bSyznrT4uA29iFgM69eOLuysUhcafKWEs130_head {
  this: np:hasAssertion dgn-np:NP280633.RAnezNV00tm5bSyznrT4uA29iFgM69eOLuysUhcafKWEs130_assertion;
    np:hasProvenance dgn-np:NP280633.RAnezNV00tm5bSyznrT4uA29iFgM69eOLuysUhcafKWEs130_provenance;
    np:hasPublicationInfo dgn-np:NP280633.RAnezNV00tm5bSyznrT4uA29iFgM69eOLuysUhcafKWEs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP280633.RAnezNV00tm5bSyznrT4uA29iFgM69eOLuysUhcafKWEs130_assertion a np:Assertion .
  
  dgn-np:NP280633.RAnezNV00tm5bSyznrT4uA29iFgM69eOLuysUhcafKWEs130_provenance a np:Provenance .
  
  dgn-np:NP280633.RAnezNV00tm5bSyznrT4uA29iFgM69eOLuysUhcafKWEs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP280633.RAnezNV00tm5bSyznrT4uA29iFgM69eOLuysUhcafKWEs130_assertion {
  miriam-gene:5468 a ncit:C16612 .
  
  lld:C0011849 a ncit:C7057 .
  
  dgn-gda:DGNa9c82cda1237d6442f45364c3d10f6e6 sio:SIO_000628 miriam-gene:5468, lld:C0011849;
    a sio:SIO_001122 .
}

dgn-np:NP280633.RAnezNV00tm5bSyznrT4uA29iFgM69eOLuysUhcafKWEs130_provenance {
  dgn-np:NP280633.RAnezNV00tm5bSyznrT4uA29iFgM69eOLuysUhcafKWEs130_assertion dcterms:description
      "[Two naturally occurring mutations in the PPAR gamma gene, Pro115Gln and Pro12Ala, have recently been shown to impair the function of the PPAR gamma2 isoform of the receptor and to be associated with obesity or diabetes-related phenotypes in different populations.]. 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:10757637;
    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:NP280633.RAnezNV00tm5bSyznrT4uA29iFgM69eOLuysUhcafKWEs130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:53+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" .
}