@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP816121.RAnqHQG1tzBblvkAtES-gWsdhWNgj7nEe2zugDB2CnMnU
> .
@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:NP816121.RAnqHQG1tzBblvkAtES-gWsdhWNgj7nEe2zugDB2CnMnU130_head
{
this:
np:hasAssertion
dgn-np:NP816121.RAnqHQG1tzBblvkAtES-gWsdhWNgj7nEe2zugDB2CnMnU130_assertion
;
np:hasProvenance
dgn-np:NP816121.RAnqHQG1tzBblvkAtES-gWsdhWNgj7nEe2zugDB2CnMnU130_provenance
;
np:hasPublicationInfo
dgn-np:NP816121.RAnqHQG1tzBblvkAtES-gWsdhWNgj7nEe2zugDB2CnMnU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP816121.RAnqHQG1tzBblvkAtES-gWsdhWNgj7nEe2zugDB2CnMnU130_assertion
a
np:Assertion
.
dgn-np:NP816121.RAnqHQG1tzBblvkAtES-gWsdhWNgj7nEe2zugDB2CnMnU130_provenance
a
np:Provenance
.
dgn-np:NP816121.RAnqHQG1tzBblvkAtES-gWsdhWNgj7nEe2zugDB2CnMnU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP816121.RAnqHQG1tzBblvkAtES-gWsdhWNgj7nEe2zugDB2CnMnU130_assertion
{
miriam-gene:4255
a
ncit:C16612
.
lld:C0029925
a
ncit:C7057
.
dgn-gda:DGN799c037a1c338a32f7526b02f9a31477
sio:SIO_000628
miriam-gene:4255
,
lld:C0029925
;
a
sio:SIO_001121
.
}
dgn-np:NP816121.RAnqHQG1tzBblvkAtES-gWsdhWNgj7nEe2zugDB2CnMnU130_provenance
{
dgn-np:NP816121.RAnqHQG1tzBblvkAtES-gWsdhWNgj7nEe2zugDB2CnMnU130_assertion
dcterms:description
"[Using a 15% cut-off for methylation, we observed significantly higher methylation in genes MGMT, PAX5, CDH13, WT1, THBS1, GATA5 in the ovarian cancer group, while in the ESR1 gene we observed significantly higher methylation in the control group compared with the ovarian cancer group.]. 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:23438850
;
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:NP816121.RAnqHQG1tzBblvkAtES-gWsdhWNgj7nEe2zugDB2CnMnU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:20+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" .
}