@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP553363.RARVd1iCaXheKyYpA1nsGjywWXCpZVDl69sO9rh2otzto> .
@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:NP553363.RARVd1iCaXheKyYpA1nsGjywWXCpZVDl69sO9rh2otzto130_head {
  this: np:hasAssertion dgn-np:NP553363.RARVd1iCaXheKyYpA1nsGjywWXCpZVDl69sO9rh2otzto130_assertion ;
    np:hasProvenance dgn-np:NP553363.RARVd1iCaXheKyYpA1nsGjywWXCpZVDl69sO9rh2otzto130_provenance ;
    np:hasPublicationInfo dgn-np:NP553363.RARVd1iCaXheKyYpA1nsGjywWXCpZVDl69sO9rh2otzto130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP553363.RARVd1iCaXheKyYpA1nsGjywWXCpZVDl69sO9rh2otzto130_assertion a np:Assertion .
  dgn-np:NP553363.RARVd1iCaXheKyYpA1nsGjywWXCpZVDl69sO9rh2otzto130_provenance a np:Provenance .
  dgn-np:NP553363.RARVd1iCaXheKyYpA1nsGjywWXCpZVDl69sO9rh2otzto130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP553363.RARVd1iCaXheKyYpA1nsGjywWXCpZVDl69sO9rh2otzto130_assertion {
  miriam-gene:2194 a ncit:C16612 .
  lld:C0079773 a ncit:C7057 .
  dgn-gda:DGNa88abbab13fcd321f17232b1d068d09f sio:SIO_000628 miriam-gene:2194 , lld:C0079773 ;
    a sio:SIO_001121 .
}
dgn-np:NP553363.RARVd1iCaXheKyYpA1nsGjywWXCpZVDl69sO9rh2otzto130_provenance {
  dgn-np:NP553363.RARVd1iCaXheKyYpA1nsGjywWXCpZVDl69sO9rh2otzto130_assertion dcterms:description "[In aggregate, these findings provide evidence that like normal T cells, CTCL cells exhibit a mechanistic connection between transcriptional regulation of FAS and sensitivity to FAS-mediated apoptosis, point to the development of FAS deficiency as one molecular mechanism responsible for acquired resistance to apoptosis in CTCL, and indicate that upregulation of FAS expression can restore sensitivity to apoptosis.]. 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:18923451 ;
    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:NP553363.RARVd1iCaXheKyYpA1nsGjywWXCpZVDl69sO9rh2otzto130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:33+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" .
}