@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP405759.RA0_LnVvGIcMtbcj4IGTnPb4ALkyhwyRMzgEcePW_G69U
> .
@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:NP405759.RA0_LnVvGIcMtbcj4IGTnPb4ALkyhwyRMzgEcePW_G69U130_head
{
this:
np:hasAssertion
dgn-np:NP405759.RA0_LnVvGIcMtbcj4IGTnPb4ALkyhwyRMzgEcePW_G69U130_assertion
;
np:hasProvenance
dgn-np:NP405759.RA0_LnVvGIcMtbcj4IGTnPb4ALkyhwyRMzgEcePW_G69U130_provenance
;
np:hasPublicationInfo
dgn-np:NP405759.RA0_LnVvGIcMtbcj4IGTnPb4ALkyhwyRMzgEcePW_G69U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP405759.RA0_LnVvGIcMtbcj4IGTnPb4ALkyhwyRMzgEcePW_G69U130_assertion
a
np:Assertion
.
dgn-np:NP405759.RA0_LnVvGIcMtbcj4IGTnPb4ALkyhwyRMzgEcePW_G69U130_provenance
a
np:Provenance
.
dgn-np:NP405759.RA0_LnVvGIcMtbcj4IGTnPb4ALkyhwyRMzgEcePW_G69U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP405759.RA0_LnVvGIcMtbcj4IGTnPb4ALkyhwyRMzgEcePW_G69U130_assertion
{
miriam-gene:142
a
ncit:C16612
.
lld:C0476089
a
ncit:C7057
.
dgn-gda:DGNb01e3d41eb751429b0d3590cc8854e00
sio:SIO_000628
miriam-gene:142
,
lld:C0476089
;
a
sio:SIO_001121
.
}
dgn-np:NP405759.RA0_LnVvGIcMtbcj4IGTnPb4ALkyhwyRMzgEcePW_G69U130_provenance
{
dgn-np:NP405759.RA0_LnVvGIcMtbcj4IGTnPb4ALkyhwyRMzgEcePW_G69U130_assertion
dcterms:description
"[Our findings imply that PARP1 overexpression may participate in endometrial cancer progression, and abnormal hypomethylation of CpG sites within the ETS motif in the core promoter region may be responsible for PARP1 overexpression in EAC tissues.]. 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:23762867
;
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:NP405759.RA0_LnVvGIcMtbcj4IGTnPb4ALkyhwyRMzgEcePW_G69U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:01+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" .
}