@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP231732.RAnfcZCW4a3H-vsh_lv-MLL3En0iHPEVDC17khQUw8r4k
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP231732.RAnfcZCW4a3H-vsh_lv-MLL3En0iHPEVDC17khQUw8r4k130_assertion
;
np:hasProvenance
dgn-np:NP231732.RAnfcZCW4a3H-vsh_lv-MLL3En0iHPEVDC17khQUw8r4k130_provenance
;
np:hasPublicationInfo
dgn-np:NP231732.RAnfcZCW4a3H-vsh_lv-MLL3En0iHPEVDC17khQUw8r4k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP231732.RAnfcZCW4a3H-vsh_lv-MLL3En0iHPEVDC17khQUw8r4k130_assertion
a
np:Assertion
.
dgn-np:NP231732.RAnfcZCW4a3H-vsh_lv-MLL3En0iHPEVDC17khQUw8r4k130_provenance
a
np:Provenance
.
dgn-np:NP231732.RAnfcZCW4a3H-vsh_lv-MLL3En0iHPEVDC17khQUw8r4k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP231732.RAnfcZCW4a3H-vsh_lv-MLL3En0iHPEVDC17khQUw8r4k130_assertion
{
miriam-gene:1786
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN5e8e23e897bfd1b65330117dc8cad535
sio:SIO_000628
miriam-gene:1786
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP231732.RAnfcZCW4a3H-vsh_lv-MLL3En0iHPEVDC17khQUw8r4k130_provenance
{
dgn-np:NP231732.RAnfcZCW4a3H-vsh_lv-MLL3En0iHPEVDC17khQUw8r4k130_assertion
dcterms:description
"[Thus, our results show the usefulness of DNMT genetic disruption strategies combined with methylated DNA immunoprecipitation in searching for unknown hypermethylated candidate genes in human cancer that might aid our understanding of the biology of the disease and be of potential translational use.]. 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:18089774
;
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:NP231732.RAnfcZCW4a3H-vsh_lv-MLL3En0iHPEVDC17khQUw8r4k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:10+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
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"v2.1.0" .
}