@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP472121.RAzHsLcWQNwyP17a08liNd7Wjd2AslJHug_WNSG5PEi0s
> .
@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:NP472121.RAzHsLcWQNwyP17a08liNd7Wjd2AslJHug_WNSG5PEi0s130_head
{
this:
np:hasAssertion
dgn-np:NP472121.RAzHsLcWQNwyP17a08liNd7Wjd2AslJHug_WNSG5PEi0s130_assertion
;
np:hasProvenance
dgn-np:NP472121.RAzHsLcWQNwyP17a08liNd7Wjd2AslJHug_WNSG5PEi0s130_provenance
;
np:hasPublicationInfo
dgn-np:NP472121.RAzHsLcWQNwyP17a08liNd7Wjd2AslJHug_WNSG5PEi0s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP472121.RAzHsLcWQNwyP17a08liNd7Wjd2AslJHug_WNSG5PEi0s130_assertion
a
np:Assertion
.
dgn-np:NP472121.RAzHsLcWQNwyP17a08liNd7Wjd2AslJHug_WNSG5PEi0s130_provenance
a
np:Provenance
.
dgn-np:NP472121.RAzHsLcWQNwyP17a08liNd7Wjd2AslJHug_WNSG5PEi0s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP472121.RAzHsLcWQNwyP17a08liNd7Wjd2AslJHug_WNSG5PEi0s130_assertion
{
miriam-gene:8932
a
ncit:C16612
.
lld:C0600139
a
ncit:C7057
.
dgn-gda:DGN2ac5e6edaaf07b78e1f8b505d4ca42ad
sio:SIO_000628
miriam-gene:8932
,
lld:C0600139
;
a
sio:SIO_001121
.
}
dgn-np:NP472121.RAzHsLcWQNwyP17a08liNd7Wjd2AslJHug_WNSG5PEi0s130_provenance
{
dgn-np:NP472121.RAzHsLcWQNwyP17a08liNd7Wjd2AslJHug_WNSG5PEi0s130_assertion
dcterms:description
"[These findings suggest that the transcriptional silencing of the 14-3-3sigma gene is caused by promoter CpG island methylation associated with MBD2, and that this 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: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:NP472121.RAzHsLcWQNwyP17a08liNd7Wjd2AslJHug_WNSG5PEi0s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:43+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" .
}