@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP275636.RAs-Lp0beX2TS9C6B38la3GI6o7XjE6QipYDeYaOd3jL4
> .
@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:NP275636.RAs-Lp0beX2TS9C6B38la3GI6o7XjE6QipYDeYaOd3jL4130_head
{
this:
np:hasAssertion
dgn-np:NP275636.RAs-Lp0beX2TS9C6B38la3GI6o7XjE6QipYDeYaOd3jL4130_assertion
;
np:hasProvenance
dgn-np:NP275636.RAs-Lp0beX2TS9C6B38la3GI6o7XjE6QipYDeYaOd3jL4130_provenance
;
np:hasPublicationInfo
dgn-np:NP275636.RAs-Lp0beX2TS9C6B38la3GI6o7XjE6QipYDeYaOd3jL4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP275636.RAs-Lp0beX2TS9C6B38la3GI6o7XjE6QipYDeYaOd3jL4130_assertion
a
np:Assertion
.
dgn-np:NP275636.RAs-Lp0beX2TS9C6B38la3GI6o7XjE6QipYDeYaOd3jL4130_provenance
a
np:Provenance
.
dgn-np:NP275636.RAs-Lp0beX2TS9C6B38la3GI6o7XjE6QipYDeYaOd3jL4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP275636.RAs-Lp0beX2TS9C6B38la3GI6o7XjE6QipYDeYaOd3jL4130_assertion
{
miriam-gene:864
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGNed7bf5ef8329816c8507ecd422e7722e
sio:SIO_000628
miriam-gene:864
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP275636.RAs-Lp0beX2TS9C6B38la3GI6o7XjE6QipYDeYaOd3jL4130_provenance
{
dgn-np:NP275636.RAs-Lp0beX2TS9C6B38la3GI6o7XjE6QipYDeYaOd3jL4130_assertion
dcterms:description
"[This study suggests that transcriptional repression of RUNX3 is caused by promoter hypermethylation of the RUNX3 CpG island in colorectal cancer cell lines, and the results of these experiments may contribute to an understanding of the role of RUNX3 inactivation in the pathogenesis of colorectal cancers.]. 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:15273736
;
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:NP275636.RAs-Lp0beX2TS9C6B38la3GI6o7XjE6QipYDeYaOd3jL4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:35+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" .
}