@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP104431.RA3BdMaHMCiE26stFc8_m5kTYpWhMwxwxJSnzauZ70310
> .
@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:NP104431.RA3BdMaHMCiE26stFc8_m5kTYpWhMwxwxJSnzauZ70310130_head
{
this:
np:hasAssertion
dgn-np:NP104431.RA3BdMaHMCiE26stFc8_m5kTYpWhMwxwxJSnzauZ70310130_assertion
;
np:hasProvenance
dgn-np:NP104431.RA3BdMaHMCiE26stFc8_m5kTYpWhMwxwxJSnzauZ70310130_provenance
;
np:hasPublicationInfo
dgn-np:NP104431.RA3BdMaHMCiE26stFc8_m5kTYpWhMwxwxJSnzauZ70310130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP104431.RA3BdMaHMCiE26stFc8_m5kTYpWhMwxwxJSnzauZ70310130_assertion
a
np:Assertion
.
dgn-np:NP104431.RA3BdMaHMCiE26stFc8_m5kTYpWhMwxwxJSnzauZ70310130_provenance
a
np:Provenance
.
dgn-np:NP104431.RA3BdMaHMCiE26stFc8_m5kTYpWhMwxwxJSnzauZ70310130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP104431.RA3BdMaHMCiE26stFc8_m5kTYpWhMwxwxJSnzauZ70310130_assertion
{
miriam-gene:25988
a
ncit:C16612
.
lld:C0033578
a
ncit:C7057
.
dgn-gda:DGN7c8b2a6dfd005e13471fedb829dc7e94
sio:SIO_000628
miriam-gene:25988
,
lld:C0033578
;
a
sio:SIO_001123
.
}
dgn-np:NP104431.RA3BdMaHMCiE26stFc8_m5kTYpWhMwxwxJSnzauZ70310130_provenance
{
dgn-np:NP104431.RA3BdMaHMCiE26stFc8_m5kTYpWhMwxwxJSnzauZ70310130_assertion
dcterms:description
"[the transcriptional silencing of the 14-3-3sigma gene is caused by promoter CpG island methylation associated with MBD2, which may play an important role in prostate cancer progression during the invasive and metastatic stages of the disease ]. 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:16786000
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP104431.RA3BdMaHMCiE26stFc8_m5kTYpWhMwxwxJSnzauZ70310130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:53+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" .
}