@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP844635.RAswozlMyPrhoZ3BqTifICjYhMBos-pPUn3oedZMyM8as
> .
@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:NP844635.RAswozlMyPrhoZ3BqTifICjYhMBos-pPUn3oedZMyM8as130_assertion
;
np:hasProvenance
dgn-np:NP844635.RAswozlMyPrhoZ3BqTifICjYhMBos-pPUn3oedZMyM8as130_provenance
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np:hasPublicationInfo
dgn-np:NP844635.RAswozlMyPrhoZ3BqTifICjYhMBos-pPUn3oedZMyM8as130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP844635.RAswozlMyPrhoZ3BqTifICjYhMBos-pPUn3oedZMyM8as130_assertion
a
np:Assertion
.
dgn-np:NP844635.RAswozlMyPrhoZ3BqTifICjYhMBos-pPUn3oedZMyM8as130_provenance
a
np:Provenance
.
dgn-np:NP844635.RAswozlMyPrhoZ3BqTifICjYhMBos-pPUn3oedZMyM8as130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP844635.RAswozlMyPrhoZ3BqTifICjYhMBos-pPUn3oedZMyM8as130_assertion
{
miriam-gene:3625
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN1074a9a83d3770e78f91920482c6737f
sio:SIO_000628
miriam-gene:3625
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP844635.RAswozlMyPrhoZ3BqTifICjYhMBos-pPUn3oedZMyM8as130_provenance
{
dgn-np:NP844635.RAswozlMyPrhoZ3BqTifICjYhMBos-pPUn3oedZMyM8as130_assertion
dcterms:description
"[Given that the number of hypermethylated loci at 2q14.2 likely affects the range of silenced flanking genes, high frequency of simultaneous hypermethylation of three CpG islands (EN1, SCTR, and INHBB) may have potential influence on specific characteristics of CIMP+ colorectal cancers.]. 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:18403637
;
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:NP844635.RAswozlMyPrhoZ3BqTifICjYhMBos-pPUn3oedZMyM8as130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:36+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
<
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> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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dgn-void:disgenetrdf
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}