@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP277570.RAOn_M5SbqIQEmEvHUtYb045LYlljphaK8broW40Drhk8
> .
@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:NP277570.RAOn_M5SbqIQEmEvHUtYb045LYlljphaK8broW40Drhk8130_head
{
this:
np:hasAssertion
dgn-np:NP277570.RAOn_M5SbqIQEmEvHUtYb045LYlljphaK8broW40Drhk8130_assertion
;
np:hasProvenance
dgn-np:NP277570.RAOn_M5SbqIQEmEvHUtYb045LYlljphaK8broW40Drhk8130_provenance
;
np:hasPublicationInfo
dgn-np:NP277570.RAOn_M5SbqIQEmEvHUtYb045LYlljphaK8broW40Drhk8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP277570.RAOn_M5SbqIQEmEvHUtYb045LYlljphaK8broW40Drhk8130_assertion
a
np:Assertion
.
dgn-np:NP277570.RAOn_M5SbqIQEmEvHUtYb045LYlljphaK8broW40Drhk8130_provenance
a
np:Provenance
.
dgn-np:NP277570.RAOn_M5SbqIQEmEvHUtYb045LYlljphaK8broW40Drhk8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP277570.RAOn_M5SbqIQEmEvHUtYb045LYlljphaK8broW40Drhk8130_assertion
{
miriam-gene:1540
a
ncit:C16612
.
lld:C1457883
a
ncit:C7057
.
dgn-gda:DGN0f89ae666b6ed72b5c743da02b4ab25e
sio:SIO_000628
miriam-gene:1540
,
lld:C1457883
;
a
sio:SIO_001121
.
}
dgn-np:NP277570.RAOn_M5SbqIQEmEvHUtYb045LYlljphaK8broW40Drhk8130_provenance
{
dgn-np:NP277570.RAOn_M5SbqIQEmEvHUtYb045LYlljphaK8broW40Drhk8130_assertion
dcterms:description
"[In contrast with previous studies showing the development of benign tumors by mutations in the CYLD gene, here we provide evidence that the occurrence of mutations in the CYLD gene in tumorigenic epidermal cells (carrying previous mutations) increases the aggressiveness of carcinomas, mainly through enhancement of the expression of angiogenic factors, having therefore a key role in epidermal cancer malignancy.]. 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:20838385
;
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:NP277570.RAOn_M5SbqIQEmEvHUtYb045LYlljphaK8broW40Drhk8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:36+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" .
}