@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP497022.RAM0R7vXHBgTnV_XwUEwq3Hg_pt3TtScYDwraYFdyaBks> .
@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:NP497022.RAM0R7vXHBgTnV_XwUEwq3Hg_pt3TtScYDwraYFdyaBks130_head {
  this: np:hasAssertion dgn-np:NP497022.RAM0R7vXHBgTnV_XwUEwq3Hg_pt3TtScYDwraYFdyaBks130_assertion;
    np:hasProvenance dgn-np:NP497022.RAM0R7vXHBgTnV_XwUEwq3Hg_pt3TtScYDwraYFdyaBks130_provenance;
    np:hasPublicationInfo dgn-np:NP497022.RAM0R7vXHBgTnV_XwUEwq3Hg_pt3TtScYDwraYFdyaBks130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP497022.RAM0R7vXHBgTnV_XwUEwq3Hg_pt3TtScYDwraYFdyaBks130_assertion a np:Assertion .
  
  dgn-np:NP497022.RAM0R7vXHBgTnV_XwUEwq3Hg_pt3TtScYDwraYFdyaBks130_provenance a np:Provenance .
  
  dgn-np:NP497022.RAM0R7vXHBgTnV_XwUEwq3Hg_pt3TtScYDwraYFdyaBks130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP497022.RAM0R7vXHBgTnV_XwUEwq3Hg_pt3TtScYDwraYFdyaBks130_assertion {
  miriam-gene:3159 a ncit:C16612 .
  
  lld:C0011860 a ncit:C7057 .
  
  dgn-gda:DGN18198d9054eb5e96005e1b89100bc278 sio:SIO_000628 miriam-gene:3159, lld:C0011860;
    a sio:SIO_001121 .
}

dgn-np:NP497022.RAM0R7vXHBgTnV_XwUEwq3Hg_pt3TtScYDwraYFdyaBks130_provenance {
  dgn-np:NP497022.RAM0R7vXHBgTnV_XwUEwq3Hg_pt3TtScYDwraYFdyaBks130_assertion dcterms:description
      "[Loss of Hmga1 expression, induced in mice by disrupting the Hmga1 gene, considerably decreased insulin receptor expression in the major targets of insulin action, largely impaired insulin signaling and severely reduced insulin secretion, causing a phenotype characteristic of human type 2 diabetes.]. 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:15924147;
    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:NP497022.RAM0R7vXHBgTnV_XwUEwq3Hg_pt3TtScYDwraYFdyaBks130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:30+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: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" .
}