@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP345644.RAuew46_gBxD3wSoYaSvz7kbxb9eYtgKQVcKW5H7U6ebU
> .
@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:NP345644.RAuew46_gBxD3wSoYaSvz7kbxb9eYtgKQVcKW5H7U6ebU130_head
{
this:
np:hasAssertion
dgn-np:NP345644.RAuew46_gBxD3wSoYaSvz7kbxb9eYtgKQVcKW5H7U6ebU130_assertion
;
np:hasProvenance
dgn-np:NP345644.RAuew46_gBxD3wSoYaSvz7kbxb9eYtgKQVcKW5H7U6ebU130_provenance
;
np:hasPublicationInfo
dgn-np:NP345644.RAuew46_gBxD3wSoYaSvz7kbxb9eYtgKQVcKW5H7U6ebU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP345644.RAuew46_gBxD3wSoYaSvz7kbxb9eYtgKQVcKW5H7U6ebU130_assertion
a
np:Assertion
.
dgn-np:NP345644.RAuew46_gBxD3wSoYaSvz7kbxb9eYtgKQVcKW5H7U6ebU130_provenance
a
np:Provenance
.
dgn-np:NP345644.RAuew46_gBxD3wSoYaSvz7kbxb9eYtgKQVcKW5H7U6ebU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP345644.RAuew46_gBxD3wSoYaSvz7kbxb9eYtgKQVcKW5H7U6ebU130_assertion
{
miriam-gene:27232
a
ncit:C16612
.
lld:C2239176
a
ncit:C7057
.
dgn-gda:DGNebc3f3fb86aae8322bb6c80604053286
sio:SIO_000628
miriam-gene:27232
,
lld:C2239176
;
a
sio:SIO_001121
.
}
dgn-np:NP345644.RAuew46_gBxD3wSoYaSvz7kbxb9eYtgKQVcKW5H7U6ebU130_provenance
{
dgn-np:NP345644.RAuew46_gBxD3wSoYaSvz7kbxb9eYtgKQVcKW5H7U6ebU130_assertion
dcterms:description
"[The findings in this manuscript indicate that DNA hypermethylation plays an important role in the repression of GNMT in HCC and that loss of GNMT in human HCC could promote the establishment of aberrant DNA methylation patterns at specific gene promoters.]. 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:23475283
;
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:NP345644.RAuew46_gBxD3wSoYaSvz7kbxb9eYtgKQVcKW5H7U6ebU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:23+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" .
}