@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP826238.RAHsMbUHDPkx1MaZ-7NmTwZw_90Akqxx78L0uQBmuBLIA> .
@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:NP826238.RAHsMbUHDPkx1MaZ-7NmTwZw_90Akqxx78L0uQBmuBLIA130_head {
  this: np:hasAssertion dgn-np:NP826238.RAHsMbUHDPkx1MaZ-7NmTwZw_90Akqxx78L0uQBmuBLIA130_assertion;
    np:hasProvenance dgn-np:NP826238.RAHsMbUHDPkx1MaZ-7NmTwZw_90Akqxx78L0uQBmuBLIA130_provenance;
    np:hasPublicationInfo dgn-np:NP826238.RAHsMbUHDPkx1MaZ-7NmTwZw_90Akqxx78L0uQBmuBLIA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP826238.RAHsMbUHDPkx1MaZ-7NmTwZw_90Akqxx78L0uQBmuBLIA130_assertion a np:Assertion .
  
  dgn-np:NP826238.RAHsMbUHDPkx1MaZ-7NmTwZw_90Akqxx78L0uQBmuBLIA130_provenance a np:Provenance .
  
  dgn-np:NP826238.RAHsMbUHDPkx1MaZ-7NmTwZw_90Akqxx78L0uQBmuBLIA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP826238.RAHsMbUHDPkx1MaZ-7NmTwZw_90Akqxx78L0uQBmuBLIA130_assertion {
  miriam-gene:208 a ncit:C16612 .
  
  lld:C0025202 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP826238.RAHsMbUHDPkx1MaZ-7NmTwZw_90Akqxx78L0uQBmuBLIA130_provenance {
  dgn-np:NP826238.RAHsMbUHDPkx1MaZ-7NmTwZw_90Akqxx78L0uQBmuBLIA130_assertion dcterms:description
      "[To determine the prevalence of AKT E17K mutations in melanoma, the most aggressive form of skin cancer, we analysed 137 human melanoma specimens and 65 human melanoma cell lines for the previously described activating mutation of AKT1, and for analogous mutations in AKT2 and AKT3.]. 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:18813315;
    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:NP826238.RAHsMbUHDPkx1MaZ-7NmTwZw_90Akqxx78L0uQBmuBLIA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:26+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}