@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP713091.RA6Lfcx1fAHpdr1SQS2D2t53AodRD7K839tfyOHNZirSw
> .
@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:NP713091.RA6Lfcx1fAHpdr1SQS2D2t53AodRD7K839tfyOHNZirSw130_head
{
this:
np:hasAssertion
dgn-np:NP713091.RA6Lfcx1fAHpdr1SQS2D2t53AodRD7K839tfyOHNZirSw130_assertion
;
np:hasProvenance
dgn-np:NP713091.RA6Lfcx1fAHpdr1SQS2D2t53AodRD7K839tfyOHNZirSw130_provenance
;
np:hasPublicationInfo
dgn-np:NP713091.RA6Lfcx1fAHpdr1SQS2D2t53AodRD7K839tfyOHNZirSw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP713091.RA6Lfcx1fAHpdr1SQS2D2t53AodRD7K839tfyOHNZirSw130_assertion
a
np:Assertion
.
dgn-np:NP713091.RA6Lfcx1fAHpdr1SQS2D2t53AodRD7K839tfyOHNZirSw130_provenance
a
np:Provenance
.
dgn-np:NP713091.RA6Lfcx1fAHpdr1SQS2D2t53AodRD7K839tfyOHNZirSw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP713091.RA6Lfcx1fAHpdr1SQS2D2t53AodRD7K839tfyOHNZirSw130_assertion
{
miriam-gene:91833
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN2c020811307dfd1f807a5978e8d1d11e
sio:SIO_000628
miriam-gene:91833
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP713091.RA6Lfcx1fAHpdr1SQS2D2t53AodRD7K839tfyOHNZirSw130_provenance
{
dgn-np:NP713091.RA6Lfcx1fAHpdr1SQS2D2t53AodRD7K839tfyOHNZirSw130_assertion
dcterms:description
"[We report in this article for the first time, that in sporadic colorectal cancer tumor DNA both the IGF2 DMR0 and DMR2 are hypomethylated, while the H19 DMR retains its monoallelic methylation pattern.]. 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:22121898
;
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:NP713091.RA6Lfcx1fAHpdr1SQS2D2t53AodRD7K839tfyOHNZirSw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:13+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" .
}