@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP781355.RAwv_3xL1eL1Jh4ASMJJlTnsnG2NsRXHs_vAWrBrTfawc> .
@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:NP781355.RAwv_3xL1eL1Jh4ASMJJlTnsnG2NsRXHs_vAWrBrTfawc130_head {
  this: np:hasAssertion dgn-np:NP781355.RAwv_3xL1eL1Jh4ASMJJlTnsnG2NsRXHs_vAWrBrTfawc130_assertion ;
    np:hasProvenance dgn-np:NP781355.RAwv_3xL1eL1Jh4ASMJJlTnsnG2NsRXHs_vAWrBrTfawc130_provenance ;
    np:hasPublicationInfo dgn-np:NP781355.RAwv_3xL1eL1Jh4ASMJJlTnsnG2NsRXHs_vAWrBrTfawc130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP781355.RAwv_3xL1eL1Jh4ASMJJlTnsnG2NsRXHs_vAWrBrTfawc130_provenance a np:Provenance .
  dgn-np:NP781355.RAwv_3xL1eL1Jh4ASMJJlTnsnG2NsRXHs_vAWrBrTfawc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP781355.RAwv_3xL1eL1Jh4ASMJJlTnsnG2NsRXHs_vAWrBrTfawc130_assertion {
  miriam-gene:10732 a ncit:C16612 .
  lld:C0017636 a ncit:C7057 .
  dgn-gda:DGN110cea520259c7c3a1fab506e3a35180 sio:SIO_000628 miriam-gene:10732 , lld:C0017636 ;
    a sio:SIO_001121 .
}
dgn-np:NP781355.RAwv_3xL1eL1Jh4ASMJJlTnsnG2NsRXHs_vAWrBrTfawc130_provenance {
  dgn-np:NP781355.RAwv_3xL1eL1Jh4ASMJJlTnsnG2NsRXHs_vAWrBrTfawc130_assertion dcterms:description "[We could also confirm overexpression of these genes in HT-29 MCTSs and in MCTSs formed by the human glioblastoma tumor cell lines U343 MG, U373 MG, and DBTRG 05 MG. Knockdown of KLF5, Erbin, DUSP11, and TCFL5 was effectively achieved after transfection of HT-29 cells with the appropriate short-interfering RNAs (siRNAs), and correlated with a significant inhibition of MCTS formation in the case of KLF5, Erbin, and TCFL5 siRNAs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP781355.RAwv_3xL1eL1Jh4ASMJJlTnsnG2NsRXHs_vAWrBrTfawc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:53+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> ;
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