@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP884129.RAshsFdDLdfDbmwk-82-KzLlUO_5Vvjaf4pozO_XH36MY
> .
@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:NP884129.RAshsFdDLdfDbmwk-82-KzLlUO_5Vvjaf4pozO_XH36MY130_head
{
this:
np:hasAssertion
dgn-np:NP884129.RAshsFdDLdfDbmwk-82-KzLlUO_5Vvjaf4pozO_XH36MY130_assertion
;
np:hasProvenance
dgn-np:NP884129.RAshsFdDLdfDbmwk-82-KzLlUO_5Vvjaf4pozO_XH36MY130_provenance
;
np:hasPublicationInfo
dgn-np:NP884129.RAshsFdDLdfDbmwk-82-KzLlUO_5Vvjaf4pozO_XH36MY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP884129.RAshsFdDLdfDbmwk-82-KzLlUO_5Vvjaf4pozO_XH36MY130_assertion
a
np:Assertion
.
dgn-np:NP884129.RAshsFdDLdfDbmwk-82-KzLlUO_5Vvjaf4pozO_XH36MY130_provenance
a
np:Provenance
.
dgn-np:NP884129.RAshsFdDLdfDbmwk-82-KzLlUO_5Vvjaf4pozO_XH36MY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP884129.RAshsFdDLdfDbmwk-82-KzLlUO_5Vvjaf4pozO_XH36MY130_assertion
{
miriam-gene:1789
a
ncit:C16612
.
lld:C0596263
a
ncit:C7057
.
dgn-gda:DGN5467553fb2b3f932cb1ec7f200b0ab0c
sio:SIO_000628
miriam-gene:1789
,
lld:C0596263
;
a
sio:SIO_001121
.
}
dgn-np:NP884129.RAshsFdDLdfDbmwk-82-KzLlUO_5Vvjaf4pozO_XH36MY130_provenance
{
dgn-np:NP884129.RAshsFdDLdfDbmwk-82-KzLlUO_5Vvjaf4pozO_XH36MY130_assertion
dcterms:description
"[The aim of this study was to detect the expression pattern of DNA methyltransferase 3B (DNMT3B) variants in primary gastric cancer (GC) and to explore the clinical significance of DNMT3B variants in gastric carcinogenesis.]. 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:20127025
;
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:NP884129.RAshsFdDLdfDbmwk-82-KzLlUO_5Vvjaf4pozO_XH36MY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:00+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" .
}