@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP527664.RAkDvofJllIud4F7WT0DBAgPqPLhuIKfj0ccv8huMcP0o
> .
@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:NP527664.RAkDvofJllIud4F7WT0DBAgPqPLhuIKfj0ccv8huMcP0o130_head
{
this:
np:hasAssertion
dgn-np:NP527664.RAkDvofJllIud4F7WT0DBAgPqPLhuIKfj0ccv8huMcP0o130_assertion
;
np:hasProvenance
dgn-np:NP527664.RAkDvofJllIud4F7WT0DBAgPqPLhuIKfj0ccv8huMcP0o130_provenance
;
np:hasPublicationInfo
dgn-np:NP527664.RAkDvofJllIud4F7WT0DBAgPqPLhuIKfj0ccv8huMcP0o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP527664.RAkDvofJllIud4F7WT0DBAgPqPLhuIKfj0ccv8huMcP0o130_assertion
a
np:Assertion
.
dgn-np:NP527664.RAkDvofJllIud4F7WT0DBAgPqPLhuIKfj0ccv8huMcP0o130_provenance
a
np:Provenance
.
dgn-np:NP527664.RAkDvofJllIud4F7WT0DBAgPqPLhuIKfj0ccv8huMcP0o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP527664.RAkDvofJllIud4F7WT0DBAgPqPLhuIKfj0ccv8huMcP0o130_assertion
{
miriam-gene:2146
a
ncit:C16612
.
lld:C0008928
a
ncit:C7057
.
dgn-gda:DGNd8c09c0ff0de13d2352c366ce9b2dd6d
sio:SIO_000628
miriam-gene:2146
,
lld:C0008928
;
a
sio:SIO_001121
.
}
dgn-np:NP527664.RAkDvofJllIud4F7WT0DBAgPqPLhuIKfj0ccv8huMcP0o130_provenance
{
dgn-np:NP527664.RAkDvofJllIud4F7WT0DBAgPqPLhuIKfj0ccv8huMcP0o130_assertion
dcterms:description
"[In lung and bladder cancer cells overexpressing EZH2, suppression of EZH2 using specific siRNAs inhibited incorporation of BrdU and resulted in significant suppression of cell growth, even though no significant effect was observed in the normal cell strain CCD-18Co, which has undetectable EZH2.]. 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:21539681
;
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:NP527664.RAkDvofJllIud4F7WT0DBAgPqPLhuIKfj0ccv8huMcP0o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:16+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" .
}