@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP498836.RAObqPpB3nlm2aRHNEsDDm7r9ZLvJZ-XD5alEIsBSAuh4
> .
@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:NP498836.RAObqPpB3nlm2aRHNEsDDm7r9ZLvJZ-XD5alEIsBSAuh4130_head
{
this:
np:hasAssertion
dgn-np:NP498836.RAObqPpB3nlm2aRHNEsDDm7r9ZLvJZ-XD5alEIsBSAuh4130_assertion
;
np:hasProvenance
dgn-np:NP498836.RAObqPpB3nlm2aRHNEsDDm7r9ZLvJZ-XD5alEIsBSAuh4130_provenance
;
np:hasPublicationInfo
dgn-np:NP498836.RAObqPpB3nlm2aRHNEsDDm7r9ZLvJZ-XD5alEIsBSAuh4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP498836.RAObqPpB3nlm2aRHNEsDDm7r9ZLvJZ-XD5alEIsBSAuh4130_assertion
a
np:Assertion
.
dgn-np:NP498836.RAObqPpB3nlm2aRHNEsDDm7r9ZLvJZ-XD5alEIsBSAuh4130_provenance
a
np:Provenance
.
dgn-np:NP498836.RAObqPpB3nlm2aRHNEsDDm7r9ZLvJZ-XD5alEIsBSAuh4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP498836.RAObqPpB3nlm2aRHNEsDDm7r9ZLvJZ-XD5alEIsBSAuh4130_assertion
{
miriam-gene:420
a
ncit:C16612
.
lld:C0699791
a
ncit:C7057
.
dgn-gda:DGNbbd488456ba6d497eac996b26fd3d6d2
sio:SIO_000628
miriam-gene:420
,
lld:C0699791
;
a
sio:SIO_001121
.
}
dgn-np:NP498836.RAObqPpB3nlm2aRHNEsDDm7r9ZLvJZ-XD5alEIsBSAuh4130_provenance
{
dgn-np:NP498836.RAObqPpB3nlm2aRHNEsDDm7r9ZLvJZ-XD5alEIsBSAuh4130_assertion
dcterms:description
"[Among differentially methylated genes, we identified new genes (CHRNA3 and DOK1) as targets of aberrant hypermethylation in GC, suggesting that epigenetic deregulation of these genes and their corresponding cellular pathways may promote the development and progression of GC.]. 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:21831520
;
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:NP498836.RAObqPpB3nlm2aRHNEsDDm7r9ZLvJZ-XD5alEIsBSAuh4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:57+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" .
}