@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP529229.RAnliS6pj4HtymLTSBjH_ixWTN4rMxxNnbrh7FglvXOEY> .
@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:NP529229.RAnliS6pj4HtymLTSBjH_ixWTN4rMxxNnbrh7FglvXOEY130_head {
  this: np:hasAssertion dgn-np:NP529229.RAnliS6pj4HtymLTSBjH_ixWTN4rMxxNnbrh7FglvXOEY130_assertion;
    np:hasProvenance dgn-np:NP529229.RAnliS6pj4HtymLTSBjH_ixWTN4rMxxNnbrh7FglvXOEY130_provenance;
    np:hasPublicationInfo dgn-np:NP529229.RAnliS6pj4HtymLTSBjH_ixWTN4rMxxNnbrh7FglvXOEY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP529229.RAnliS6pj4HtymLTSBjH_ixWTN4rMxxNnbrh7FglvXOEY130_assertion a np:Assertion .
  
  dgn-np:NP529229.RAnliS6pj4HtymLTSBjH_ixWTN4rMxxNnbrh7FglvXOEY130_provenance a np:Provenance .
  
  dgn-np:NP529229.RAnliS6pj4HtymLTSBjH_ixWTN4rMxxNnbrh7FglvXOEY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP529229.RAnliS6pj4HtymLTSBjH_ixWTN4rMxxNnbrh7FglvXOEY130_assertion {
  miriam-gene:9370 a ncit:C16612 .
  
  lld:C0011860 a ncit:C7057 .
  
  dgn-gda:DGN48c36d69376ddd3cdc3a9a464286eaf6 sio:SIO_000628 miriam-gene:9370, lld:C0011860;
    a sio:SIO_001121 .
}

dgn-np:NP529229.RAnliS6pj4HtymLTSBjH_ixWTN4rMxxNnbrh7FglvXOEY130_provenance {
  dgn-np:NP529229.RAnliS6pj4HtymLTSBjH_ixWTN4rMxxNnbrh7FglvXOEY130_assertion dcterms:description
      "[Some of the common polymorphisms in the promoter region, exon and intron 2, and the rare nonsynonymous mutations in exon 3 of the human adiponectin gene were repeatedly shown in many studies from many different ethnic populations to associate with the phenotypes related to body weight, glucose metabolism, insulin sensitivity, and risk of type 2 diabetes mellitus and coronary artery 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:16389553;
    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:NP529229.RAnliS6pj4HtymLTSBjH_ixWTN4rMxxNnbrh7FglvXOEY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:44+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" .
}