@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP570756.RA3snR7DT9e3oPZcfmPqhQGRGuxiEZdfUMuufelQ9qktI
> .
@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:NP570756.RA3snR7DT9e3oPZcfmPqhQGRGuxiEZdfUMuufelQ9qktI130_head
{
this:
np:hasAssertion
dgn-np:NP570756.RA3snR7DT9e3oPZcfmPqhQGRGuxiEZdfUMuufelQ9qktI130_assertion
;
np:hasProvenance
dgn-np:NP570756.RA3snR7DT9e3oPZcfmPqhQGRGuxiEZdfUMuufelQ9qktI130_provenance
;
np:hasPublicationInfo
dgn-np:NP570756.RA3snR7DT9e3oPZcfmPqhQGRGuxiEZdfUMuufelQ9qktI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP570756.RA3snR7DT9e3oPZcfmPqhQGRGuxiEZdfUMuufelQ9qktI130_assertion
a
np:Assertion
.
dgn-np:NP570756.RA3snR7DT9e3oPZcfmPqhQGRGuxiEZdfUMuufelQ9qktI130_provenance
a
np:Provenance
.
dgn-np:NP570756.RA3snR7DT9e3oPZcfmPqhQGRGuxiEZdfUMuufelQ9qktI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP570756.RA3snR7DT9e3oPZcfmPqhQGRGuxiEZdfUMuufelQ9qktI130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C1260386
a
ncit:C7057
.
dgn-gda:DGNc3bd4fb80f8dd0c30369ffe955c68866
sio:SIO_000628
miriam-gene:1080
,
lld:C1260386
;
a
sio:SIO_001121
.
}
dgn-np:NP570756.RA3snR7DT9e3oPZcfmPqhQGRGuxiEZdfUMuufelQ9qktI130_provenance
{
dgn-np:NP570756.RA3snR7DT9e3oPZcfmPqhQGRGuxiEZdfUMuufelQ9qktI130_assertion
dcterms:description
"[Understanding that the cystic fibrosis transmembrane conductance regulator (CFTR) is responsible for glutathione (GSH) transport, the authors hypothesize that mutations of the CFTR, which create abnormal GSH transport, will lead to aberrations of GSH levels in both the intracellular as well as the extracellular milieu.]. 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:16934416
;
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:NP570756.RA3snR7DT9e3oPZcfmPqhQGRGuxiEZdfUMuufelQ9qktI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:44+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" .
}