@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP697683.RAOmh0Xt-GVNAutg0hMhekHz0lQv8_99KGREHmoQKjliM
> .
@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:NP697683.RAOmh0Xt-GVNAutg0hMhekHz0lQv8_99KGREHmoQKjliM130_head
{
this:
np:hasAssertion
dgn-np:NP697683.RAOmh0Xt-GVNAutg0hMhekHz0lQv8_99KGREHmoQKjliM130_assertion
;
np:hasProvenance
dgn-np:NP697683.RAOmh0Xt-GVNAutg0hMhekHz0lQv8_99KGREHmoQKjliM130_provenance
;
np:hasPublicationInfo
dgn-np:NP697683.RAOmh0Xt-GVNAutg0hMhekHz0lQv8_99KGREHmoQKjliM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP697683.RAOmh0Xt-GVNAutg0hMhekHz0lQv8_99KGREHmoQKjliM130_assertion
a
np:Assertion
.
dgn-np:NP697683.RAOmh0Xt-GVNAutg0hMhekHz0lQv8_99KGREHmoQKjliM130_provenance
a
np:Provenance
.
dgn-np:NP697683.RAOmh0Xt-GVNAutg0hMhekHz0lQv8_99KGREHmoQKjliM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP697683.RAOmh0Xt-GVNAutg0hMhekHz0lQv8_99KGREHmoQKjliM130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C1260386
a
ncit:C7057
.
dgn-gda:DGN1b85e638069b9d7ec2e3874e6941a65d
sio:SIO_000628
miriam-gene:1080
,
lld:C1260386
;
a
sio:SIO_001121
.
}
dgn-np:NP697683.RAOmh0Xt-GVNAutg0hMhekHz0lQv8_99KGREHmoQKjliM130_provenance
{
dgn-np:NP697683.RAOmh0Xt-GVNAutg0hMhekHz0lQv8_99KGREHmoQKjliM130_assertion
dcterms:description
"[While the expression of cystic fibrosis transmembrane conductance regulator (CFTR) is restricted to the biliary epithelium in the liver, recent findings indicate that CFTR modulates reduced glutathione (GSH) transport and that CFTR dysfunction creates an imbalance in the antioxidant defense.]. 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:12297838
;
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:NP697683.RAOmh0Xt-GVNAutg0hMhekHz0lQv8_99KGREHmoQKjliM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:04+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" .
}