@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP258696.RAbtQoIOyWzrWTZafSiu5n5ew1SV-9XVEhBrGHK1dHaPw
> .
@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:NP258696.RAbtQoIOyWzrWTZafSiu5n5ew1SV-9XVEhBrGHK1dHaPw130_head
{
this:
np:hasAssertion
dgn-np:NP258696.RAbtQoIOyWzrWTZafSiu5n5ew1SV-9XVEhBrGHK1dHaPw130_assertion
;
np:hasProvenance
dgn-np:NP258696.RAbtQoIOyWzrWTZafSiu5n5ew1SV-9XVEhBrGHK1dHaPw130_provenance
;
np:hasPublicationInfo
dgn-np:NP258696.RAbtQoIOyWzrWTZafSiu5n5ew1SV-9XVEhBrGHK1dHaPw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP258696.RAbtQoIOyWzrWTZafSiu5n5ew1SV-9XVEhBrGHK1dHaPw130_assertion
a
np:Assertion
.
dgn-np:NP258696.RAbtQoIOyWzrWTZafSiu5n5ew1SV-9XVEhBrGHK1dHaPw130_provenance
a
np:Provenance
.
dgn-np:NP258696.RAbtQoIOyWzrWTZafSiu5n5ew1SV-9XVEhBrGHK1dHaPw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP258696.RAbtQoIOyWzrWTZafSiu5n5ew1SV-9XVEhBrGHK1dHaPw130_assertion
{
miriam-gene:864
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNe61a2884c1197f4ad906758fb4fb346d
sio:SIO_000628
miriam-gene:864
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP258696.RAbtQoIOyWzrWTZafSiu5n5ew1SV-9XVEhBrGHK1dHaPw130_provenance
{
dgn-np:NP258696.RAbtQoIOyWzrWTZafSiu5n5ew1SV-9XVEhBrGHK1dHaPw130_assertion
dcterms:description
"[Epigenetic changes in the methylation of the RUNX3 proximal promoter, but not common genetic changes in RUNX3, have been associated with both changes in the gene expression and development of the cancer.]. 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:21523770
;
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:NP258696.RAbtQoIOyWzrWTZafSiu5n5ew1SV-9XVEhBrGHK1dHaPw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:24+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" .
}