@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP635965.RA4NNS_VIhIOO6JMWm8BvXG-hZ9IC98ArwSwn97NXwUgo
> .
@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:NP635965.RA4NNS_VIhIOO6JMWm8BvXG-hZ9IC98ArwSwn97NXwUgo130_head
{
this:
np:hasAssertion
dgn-np:NP635965.RA4NNS_VIhIOO6JMWm8BvXG-hZ9IC98ArwSwn97NXwUgo130_assertion
;
np:hasProvenance
dgn-np:NP635965.RA4NNS_VIhIOO6JMWm8BvXG-hZ9IC98ArwSwn97NXwUgo130_provenance
;
np:hasPublicationInfo
dgn-np:NP635965.RA4NNS_VIhIOO6JMWm8BvXG-hZ9IC98ArwSwn97NXwUgo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP635965.RA4NNS_VIhIOO6JMWm8BvXG-hZ9IC98ArwSwn97NXwUgo130_assertion
a
np:Assertion
.
dgn-np:NP635965.RA4NNS_VIhIOO6JMWm8BvXG-hZ9IC98ArwSwn97NXwUgo130_provenance
a
np:Provenance
.
dgn-np:NP635965.RA4NNS_VIhIOO6JMWm8BvXG-hZ9IC98ArwSwn97NXwUgo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP635965.RA4NNS_VIhIOO6JMWm8BvXG-hZ9IC98ArwSwn97NXwUgo130_assertion
{
miriam-gene:57045
a
ncit:C16612
.
lld:C0596263
a
ncit:C7057
.
dgn-gda:DGN6d1973f24fec5d154590e9a63cfce413
sio:SIO_000628
miriam-gene:57045
,
lld:C0596263
;
a
sio:SIO_001121
.
}
dgn-np:NP635965.RA4NNS_VIhIOO6JMWm8BvXG-hZ9IC98ArwSwn97NXwUgo130_provenance
{
dgn-np:NP635965.RA4NNS_VIhIOO6JMWm8BvXG-hZ9IC98ArwSwn97NXwUgo130_assertion
dcterms:description
"[Changes in genomic methylation and its significance in carcinogenesis is in the spotlight once again, though the focus is not on the usual suspects, DNA hypermethylation and tumour suppressor gene (TSG) silencing.]. 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:14628069
;
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:NP635965.RA4NNS_VIhIOO6JMWm8BvXG-hZ9IC98ArwSwn97NXwUgo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:23+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" .
}