@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP504132.RAoBYvYehHjfEgI5mQ_h7mfOM_B9fl-ImkvZ_zWC4J-Cg
> .
@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:NP504132.RAoBYvYehHjfEgI5mQ_h7mfOM_B9fl-ImkvZ_zWC4J-Cg130_head
{
this:
np:hasAssertion
dgn-np:NP504132.RAoBYvYehHjfEgI5mQ_h7mfOM_B9fl-ImkvZ_zWC4J-Cg130_assertion
;
np:hasProvenance
dgn-np:NP504132.RAoBYvYehHjfEgI5mQ_h7mfOM_B9fl-ImkvZ_zWC4J-Cg130_provenance
;
np:hasPublicationInfo
dgn-np:NP504132.RAoBYvYehHjfEgI5mQ_h7mfOM_B9fl-ImkvZ_zWC4J-Cg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP504132.RAoBYvYehHjfEgI5mQ_h7mfOM_B9fl-ImkvZ_zWC4J-Cg130_assertion
a
np:Assertion
.
dgn-np:NP504132.RAoBYvYehHjfEgI5mQ_h7mfOM_B9fl-ImkvZ_zWC4J-Cg130_provenance
a
np:Provenance
.
dgn-np:NP504132.RAoBYvYehHjfEgI5mQ_h7mfOM_B9fl-ImkvZ_zWC4J-Cg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP504132.RAoBYvYehHjfEgI5mQ_h7mfOM_B9fl-ImkvZ_zWC4J-Cg130_assertion
{
miriam-gene:23619
a
ncit:C16612
.
lld:C0017638
a
ncit:C7057
.
dgn-gda:DGNbae999acfc8ba296a39d26107efe2a03
sio:SIO_000628
miriam-gene:23619
,
lld:C0017638
;
a
sio:SIO_001121
.
}
dgn-np:NP504132.RAoBYvYehHjfEgI5mQ_h7mfOM_B9fl-ImkvZ_zWC4J-Cg130_provenance
{
dgn-np:NP504132.RAoBYvYehHjfEgI5mQ_h7mfOM_B9fl-ImkvZ_zWC4J-Cg130_assertion
dcterms:description
"[In this article, we report that the epigenetic silencing of PEG3 expression in glioma cell lines depends on aberrant DNA methylation of an exonic CpG island, suggesting that PEG3 contributes to glioma carcinogenesis in certain cases.]. 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:11398192
;
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:NP504132.RAoBYvYehHjfEgI5mQ_h7mfOM_B9fl-ImkvZ_zWC4J-Cg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:00+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" .
}