@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP406489.RAg67nQQ4F0wjmVQ6TMs56lzaEFYZjI3ZPsGeg9Wrsvq8> .
@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:NP406489.RAg67nQQ4F0wjmVQ6TMs56lzaEFYZjI3ZPsGeg9Wrsvq8130_head {
  this: np:hasAssertion dgn-np:NP406489.RAg67nQQ4F0wjmVQ6TMs56lzaEFYZjI3ZPsGeg9Wrsvq8130_assertion;
    np:hasProvenance dgn-np:NP406489.RAg67nQQ4F0wjmVQ6TMs56lzaEFYZjI3ZPsGeg9Wrsvq8130_provenance;
    np:hasPublicationInfo dgn-np:NP406489.RAg67nQQ4F0wjmVQ6TMs56lzaEFYZjI3ZPsGeg9Wrsvq8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP406489.RAg67nQQ4F0wjmVQ6TMs56lzaEFYZjI3ZPsGeg9Wrsvq8130_assertion a np:Assertion .
  
  dgn-np:NP406489.RAg67nQQ4F0wjmVQ6TMs56lzaEFYZjI3ZPsGeg9Wrsvq8130_provenance a np:Provenance .
  
  dgn-np:NP406489.RAg67nQQ4F0wjmVQ6TMs56lzaEFYZjI3ZPsGeg9Wrsvq8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP406489.RAg67nQQ4F0wjmVQ6TMs56lzaEFYZjI3ZPsGeg9Wrsvq8130_assertion {
  miriam-gene:5295 a ncit:C16612 .
  
  lld:C0011860 a ncit:C7057 .
  
  dgn-gda:DGNa1f3e2ac00ec2d9e9b7a7ac1e2edb183 sio:SIO_000628 miriam-gene:5295, lld:C0011860;
    a sio:SIO_001121 .
}

dgn-np:NP406489.RAg67nQQ4F0wjmVQ6TMs56lzaEFYZjI3ZPsGeg9Wrsvq8130_provenance {
  dgn-np:NP406489.RAg67nQQ4F0wjmVQ6TMs56lzaEFYZjI3ZPsGeg9Wrsvq8130_assertion dcterms:description
      "[The p85alpha subunit of phosphatidyl inositol 3 kinase (PIK3R1) and the regulatory subunit 3 of protein phosphatase 1 (PPP1R3) were selected as candidate genes because both encode key proteins involved in insulin signalling and because polymorphisms in these genes have been previously implicated in insulin resistance or type II 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:12185156;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP406489.RAg67nQQ4F0wjmVQ6TMs56lzaEFYZjI3ZPsGeg9Wrsvq8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:02+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" .
}