@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP176678.RAfBH84_KLGqaPMMCTTwUXsp0pLYM3nYWYYm4WYbBksyY> .
@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:NP176678.RAfBH84_KLGqaPMMCTTwUXsp0pLYM3nYWYYm4WYbBksyY130_head {
  this: np:hasAssertion dgn-np:NP176678.RAfBH84_KLGqaPMMCTTwUXsp0pLYM3nYWYYm4WYbBksyY130_assertion;
    np:hasProvenance dgn-np:NP176678.RAfBH84_KLGqaPMMCTTwUXsp0pLYM3nYWYYm4WYbBksyY130_provenance;
    np:hasPublicationInfo dgn-np:NP176678.RAfBH84_KLGqaPMMCTTwUXsp0pLYM3nYWYYm4WYbBksyY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP176678.RAfBH84_KLGqaPMMCTTwUXsp0pLYM3nYWYYm4WYbBksyY130_assertion a np:Assertion .
  
  dgn-np:NP176678.RAfBH84_KLGqaPMMCTTwUXsp0pLYM3nYWYYm4WYbBksyY130_provenance a np:Provenance .
  
  dgn-np:NP176678.RAfBH84_KLGqaPMMCTTwUXsp0pLYM3nYWYYm4WYbBksyY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP176678.RAfBH84_KLGqaPMMCTTwUXsp0pLYM3nYWYYm4WYbBksyY130_assertion {
  miriam-gene:208 a ncit:C16612 .
  
  lld:C0220989 a ncit:C7057 .
  
  dgn-gda:DGNdf58d31c5a050bd35ac914918bfc59d1 sio:SIO_000628 miriam-gene:208, lld:C0220989;
    a sio:SIO_001121 .
}

dgn-np:NP176678.RAfBH84_KLGqaPMMCTTwUXsp0pLYM3nYWYYm4WYbBksyY130_provenance {
  dgn-np:NP176678.RAfBH84_KLGqaPMMCTTwUXsp0pLYM3nYWYYm4WYbBksyY130_assertion dcterms:description
      "[To determine whether genetic variation in AKT2 plays a broader role in human metabolic disease, we sequenced the entire coding region and splice junctions of AKT2 in 94 unrelated patients with severe insulin resistance, 35 of whom had partial lipodystrophy.]. 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:17327441;
    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:NP176678.RAfBH84_KLGqaPMMCTTwUXsp0pLYM3nYWYYm4WYbBksyY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:35+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" .
}