@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP544993.RAeeW06HDKa8pDfhom1EdiEeio21-L7Vu4s2eDMf_L6ek> .
@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:NP544993.RAeeW06HDKa8pDfhom1EdiEeio21-L7Vu4s2eDMf_L6ek130_head {
  this: np:hasAssertion dgn-np:NP544993.RAeeW06HDKa8pDfhom1EdiEeio21-L7Vu4s2eDMf_L6ek130_assertion;
    np:hasProvenance dgn-np:NP544993.RAeeW06HDKa8pDfhom1EdiEeio21-L7Vu4s2eDMf_L6ek130_provenance;
    np:hasPublicationInfo dgn-np:NP544993.RAeeW06HDKa8pDfhom1EdiEeio21-L7Vu4s2eDMf_L6ek130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP544993.RAeeW06HDKa8pDfhom1EdiEeio21-L7Vu4s2eDMf_L6ek130_assertion a np:Assertion .
  
  dgn-np:NP544993.RAeeW06HDKa8pDfhom1EdiEeio21-L7Vu4s2eDMf_L6ek130_provenance a np:Provenance .
  
  dgn-np:NP544993.RAeeW06HDKa8pDfhom1EdiEeio21-L7Vu4s2eDMf_L6ek130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP544993.RAeeW06HDKa8pDfhom1EdiEeio21-L7Vu4s2eDMf_L6ek130_assertion {
  miriam-gene:207 a ncit:C16612 .
  
  lld:C0037579 a ncit:C7057 .
  
  dgn-gda:DGNae3104cf66884359df5aa95180f231a9 sio:SIO_000628 miriam-gene:207, lld:C0037579;
    a sio:SIO_001121 .
}

dgn-np:NP544993.RAeeW06HDKa8pDfhom1EdiEeio21-L7Vu4s2eDMf_L6ek130_provenance {
  dgn-np:NP544993.RAeeW06HDKa8pDfhom1EdiEeio21-L7Vu4s2eDMf_L6ek130_assertion dcterms:description
      "[To clarify the aberrations of AKT genes, their protein products and clinicopathologic significance in bone and soft tissue tumors, expression profiles of total Akt, its isoforms and activated Akt, and increases in copy number of AKT1/AKT2 genes were examined.]. 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:24321521;
    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:NP544993.RAeeW06HDKa8pDfhom1EdiEeio21-L7Vu4s2eDMf_L6ek130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:28+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" .
}