@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP231801.RAJrA-EY2uxdw4-LeFMHKD0x_Le80m5YDPUm5JXv5Hkvs> .
@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/v3.0.0/void/> .

dgn-np:NP231801.RAJrA-EY2uxdw4-LeFMHKD0x_Le80m5YDPUm5JXv5Hkvs130_head {
  this: np:hasAssertion dgn-np:NP231801.RAJrA-EY2uxdw4-LeFMHKD0x_Le80m5YDPUm5JXv5Hkvs130_assertion;
    np:hasProvenance dgn-np:NP231801.RAJrA-EY2uxdw4-LeFMHKD0x_Le80m5YDPUm5JXv5Hkvs130_provenance;
    np:hasPublicationInfo dgn-np:NP231801.RAJrA-EY2uxdw4-LeFMHKD0x_Le80m5YDPUm5JXv5Hkvs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP231801.RAJrA-EY2uxdw4-LeFMHKD0x_Le80m5YDPUm5JXv5Hkvs130_assertion a np:Assertion .
  
  dgn-np:NP231801.RAJrA-EY2uxdw4-LeFMHKD0x_Le80m5YDPUm5JXv5Hkvs130_provenance a np:Provenance .
  
  dgn-np:NP231801.RAJrA-EY2uxdw4-LeFMHKD0x_Le80m5YDPUm5JXv5Hkvs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP231801.RAJrA-EY2uxdw4-LeFMHKD0x_Le80m5YDPUm5JXv5Hkvs130_assertion {
  miriam-gene:207 a ncit:C16612 .
  
  lld:C0002895 a ncit:C7057 .
  
  dgn-gda:DGNd6e5e681fdd104a5649ec22ba367856b sio:SIO_000628 miriam-gene:207, lld:C0002895;
    a sio:SIO_001121 .
}

dgn-np:NP231801.RAJrA-EY2uxdw4-LeFMHKD0x_Le80m5YDPUm5JXv5Hkvs130_provenance {
  dgn-np:NP231801.RAJrA-EY2uxdw4-LeFMHKD0x_Le80m5YDPUm5JXv5Hkvs130_assertion dcterms:description
      "[We found that the basal phosphorylation levels of AKT isoforms were markedly increased in neutrophils and platelets isolated from patients with sickle cell disease (SCD), an inherited hematological disorder associated with vascular inflammation and occlusion.]. 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:24642468;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP231801.RAJrA-EY2uxdw4-LeFMHKD0x_Le80m5YDPUm5JXv5Hkvs130_publicationInfo {
  this: dcterms:created "2015-08-25T14:39:52+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}