@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP223971.RAv_sa2Djg70QuPgoTJ2DnGADoBnFzZ9PqJrScDJ-mdok
> .
@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:NP223971.RAv_sa2Djg70QuPgoTJ2DnGADoBnFzZ9PqJrScDJ-mdok130_head
{
this:
np:hasAssertion
dgn-np:NP223971.RAv_sa2Djg70QuPgoTJ2DnGADoBnFzZ9PqJrScDJ-mdok130_assertion
;
np:hasProvenance
dgn-np:NP223971.RAv_sa2Djg70QuPgoTJ2DnGADoBnFzZ9PqJrScDJ-mdok130_provenance
;
np:hasPublicationInfo
dgn-np:NP223971.RAv_sa2Djg70QuPgoTJ2DnGADoBnFzZ9PqJrScDJ-mdok130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP223971.RAv_sa2Djg70QuPgoTJ2DnGADoBnFzZ9PqJrScDJ-mdok130_assertion
a
np:Assertion
.
dgn-np:NP223971.RAv_sa2Djg70QuPgoTJ2DnGADoBnFzZ9PqJrScDJ-mdok130_provenance
a
np:Provenance
.
dgn-np:NP223971.RAv_sa2Djg70QuPgoTJ2DnGADoBnFzZ9PqJrScDJ-mdok130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP223971.RAv_sa2Djg70QuPgoTJ2DnGADoBnFzZ9PqJrScDJ-mdok130_assertion
{
miriam-gene:10249
a
ncit:C16612
.
lld:C1260386
a
ncit:C7057
.
dgn-gda:DGNd5035863f6b847c713394c9fd0947f90
sio:SIO_000628
miriam-gene:10249
,
lld:C1260386
;
a
sio:SIO_001121
.
}
dgn-np:NP223971.RAv_sa2Djg70QuPgoTJ2DnGADoBnFzZ9PqJrScDJ-mdok130_provenance
{
dgn-np:NP223971.RAv_sa2Djg70QuPgoTJ2DnGADoBnFzZ9PqJrScDJ-mdok130_assertion
dcterms:description
"[In higher GSH deficiency (> 40 %) with increased ROS generation, Cp expression was decreased due to promotion of Cp mRNA decay mediated by 3'untranslated region (3'UTR) as found by transfecting chimera of chloramphenicol acetyl transferase (CAT) gene with Cp 3'UTR.]. 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:20211720
;
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:NP223971.RAv_sa2Djg70QuPgoTJ2DnGADoBnFzZ9PqJrScDJ-mdok130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:04+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" .
}