@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP809194.RARUIOxhJ5dAymd_jkKNeQ12j4aE6CjX9OAVVYq7wm4WE> .
@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:NP809194.RARUIOxhJ5dAymd_jkKNeQ12j4aE6CjX9OAVVYq7wm4WE130_head {
  this: np:hasAssertion dgn-np:NP809194.RARUIOxhJ5dAymd_jkKNeQ12j4aE6CjX9OAVVYq7wm4WE130_assertion ;
    np:hasProvenance dgn-np:NP809194.RARUIOxhJ5dAymd_jkKNeQ12j4aE6CjX9OAVVYq7wm4WE130_provenance ;
    np:hasPublicationInfo dgn-np:NP809194.RARUIOxhJ5dAymd_jkKNeQ12j4aE6CjX9OAVVYq7wm4WE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP809194.RARUIOxhJ5dAymd_jkKNeQ12j4aE6CjX9OAVVYq7wm4WE130_assertion a np:Assertion .
  dgn-np:NP809194.RARUIOxhJ5dAymd_jkKNeQ12j4aE6CjX9OAVVYq7wm4WE130_provenance a np:Provenance .
  dgn-np:NP809194.RARUIOxhJ5dAymd_jkKNeQ12j4aE6CjX9OAVVYq7wm4WE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP809194.RARUIOxhJ5dAymd_jkKNeQ12j4aE6CjX9OAVVYq7wm4WE130_assertion {
  miriam-gene:207 a ncit:C16612 .
  lld:C0027651 a ncit:C7057 .
  dgn-gda:DGN32a4e7e7d51d70bdcdc0b52674c33157 sio:SIO_000628 miriam-gene:207 , lld:C0027651 ;
    a sio:SIO_001121 .
}
dgn-np:NP809194.RARUIOxhJ5dAymd_jkKNeQ12j4aE6CjX9OAVVYq7wm4WE130_provenance {
  dgn-np:NP809194.RARUIOxhJ5dAymd_jkKNeQ12j4aE6CjX9OAVVYq7wm4WE130_assertion dcterms:description "[We also investigated aberrant expressions of phosphorylated AKT, phosphatase and tensin homolog (PTEN), tumor protein 53 (TP53), SMAD4, and CTNNB1 in 11 cases of ITPNs and compared these data with those of 50 cases of intraductal papillary mucinous neoplasm (IPMN), another distinct variant of pancreatic intraductal neoplasms.]. 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:21945955 ;
    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:NP809194.RARUIOxhJ5dAymd_jkKNeQ12j4aE6CjX9OAVVYq7wm4WE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:16+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" .
}