@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" .
}