@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP763703.RADsK9cKK6yEd4mDmQP6STX0TOP9f0FZIIiyIx3Swc_6Y
> .
@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:NP763703.RADsK9cKK6yEd4mDmQP6STX0TOP9f0FZIIiyIx3Swc_6Y130_head
{
this:
np:hasAssertion
dgn-np:NP763703.RADsK9cKK6yEd4mDmQP6STX0TOP9f0FZIIiyIx3Swc_6Y130_assertion
;
np:hasProvenance
dgn-np:NP763703.RADsK9cKK6yEd4mDmQP6STX0TOP9f0FZIIiyIx3Swc_6Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP763703.RADsK9cKK6yEd4mDmQP6STX0TOP9f0FZIIiyIx3Swc_6Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP763703.RADsK9cKK6yEd4mDmQP6STX0TOP9f0FZIIiyIx3Swc_6Y130_assertion
a
np:Assertion
.
dgn-np:NP763703.RADsK9cKK6yEd4mDmQP6STX0TOP9f0FZIIiyIx3Swc_6Y130_provenance
a
np:Provenance
.
dgn-np:NP763703.RADsK9cKK6yEd4mDmQP6STX0TOP9f0FZIIiyIx3Swc_6Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP763703.RADsK9cKK6yEd4mDmQP6STX0TOP9f0FZIIiyIx3Swc_6Y130_assertion
{
miriam-gene:898
a
ncit:C16612
.
lld:C0026764
a
ncit:C7057
.
dgn-gda:DGNc97b538d028c00a9af68b636267d9813
sio:SIO_000628
miriam-gene:898
,
lld:C0026764
;
a
sio:SIO_001121
.
}
dgn-np:NP763703.RADsK9cKK6yEd4mDmQP6STX0TOP9f0FZIIiyIx3Swc_6Y130_provenance
{
dgn-np:NP763703.RADsK9cKK6yEd4mDmQP6STX0TOP9f0FZIIiyIx3Swc_6Y130_assertion
dcterms:description
"[Ectopic over expression of CCNE1 resulted in reduced sensitivity of the MM tumor cells in comparison to the paternal cell line, whereas CCNE1 silencing with siRNA increased the cell sensitivity to seliciclib.]. 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:22558078
;
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:NP763703.RADsK9cKK6yEd4mDmQP6STX0TOP9f0FZIIiyIx3Swc_6Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:42+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" .
}