@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP879487.RADJd1u6l55G-VZGWE07vvqgDwgV_rr5GeG-Rm8ZK8kmg
> .
@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:NP879487.RADJd1u6l55G-VZGWE07vvqgDwgV_rr5GeG-Rm8ZK8kmg130_head
{
this:
np:hasAssertion
dgn-np:NP879487.RADJd1u6l55G-VZGWE07vvqgDwgV_rr5GeG-Rm8ZK8kmg130_assertion
;
np:hasProvenance
dgn-np:NP879487.RADJd1u6l55G-VZGWE07vvqgDwgV_rr5GeG-Rm8ZK8kmg130_provenance
;
np:hasPublicationInfo
dgn-np:NP879487.RADJd1u6l55G-VZGWE07vvqgDwgV_rr5GeG-Rm8ZK8kmg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP879487.RADJd1u6l55G-VZGWE07vvqgDwgV_rr5GeG-Rm8ZK8kmg130_assertion
a
np:Assertion
.
dgn-np:NP879487.RADJd1u6l55G-VZGWE07vvqgDwgV_rr5GeG-Rm8ZK8kmg130_provenance
a
np:Provenance
.
dgn-np:NP879487.RADJd1u6l55G-VZGWE07vvqgDwgV_rr5GeG-Rm8ZK8kmg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP879487.RADJd1u6l55G-VZGWE07vvqgDwgV_rr5GeG-Rm8ZK8kmg130_assertion
{
miriam-gene:6513
a
ncit:C16612
.
lld:C0020615
a
ncit:C7057
.
dgn-gda:DGN24697ef8c29fe29200fe2274bf979b2d
sio:SIO_000628
miriam-gene:6513
,
lld:C0020615
;
a
sio:SIO_001121
.
}
dgn-np:NP879487.RADJd1u6l55G-VZGWE07vvqgDwgV_rr5GeG-Rm8ZK8kmg130_provenance
{
dgn-np:NP879487.RADJd1u6l55G-VZGWE07vvqgDwgV_rr5GeG-Rm8ZK8kmg130_assertion
dcterms:description
"[Because glucose transport across these barriers is mediated exclusively by the sodium-independent glucose transporter GLUT1, changes in endothelial glucose transport and GLUT1 abundance in the barriers of the brain and retina may have profound consequences on glucose delivery to these tissues and major implications in the development of two major diabetic complications, namely insulin-induced hypoglycemia and diabetic retinopathy.]. 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:10495475
;
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:NP879487.RADJd1u6l55G-VZGWE07vvqgDwgV_rr5GeG-Rm8ZK8kmg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:57+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" .
}