@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP724703.RAdpgDLdYMWYVipfg1RKcCs3LpXwOyzPpHAz0MHJj3EqU
> .
@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:NP724703.RAdpgDLdYMWYVipfg1RKcCs3LpXwOyzPpHAz0MHJj3EqU130_head
{
this:
np:hasAssertion
dgn-np:NP724703.RAdpgDLdYMWYVipfg1RKcCs3LpXwOyzPpHAz0MHJj3EqU130_assertion
;
np:hasProvenance
dgn-np:NP724703.RAdpgDLdYMWYVipfg1RKcCs3LpXwOyzPpHAz0MHJj3EqU130_provenance
;
np:hasPublicationInfo
dgn-np:NP724703.RAdpgDLdYMWYVipfg1RKcCs3LpXwOyzPpHAz0MHJj3EqU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP724703.RAdpgDLdYMWYVipfg1RKcCs3LpXwOyzPpHAz0MHJj3EqU130_assertion
a
np:Assertion
.
dgn-np:NP724703.RAdpgDLdYMWYVipfg1RKcCs3LpXwOyzPpHAz0MHJj3EqU130_provenance
a
np:Provenance
.
dgn-np:NP724703.RAdpgDLdYMWYVipfg1RKcCs3LpXwOyzPpHAz0MHJj3EqU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP724703.RAdpgDLdYMWYVipfg1RKcCs3LpXwOyzPpHAz0MHJj3EqU130_assertion
{
miriam-gene:6527
a
ncit:C16612
.
lld:C0027721
a
ncit:C7057
.
dgn-gda:DGNf87a209bba2ead930707a6a8c64db52a
sio:SIO_000628
miriam-gene:6527
,
lld:C0027721
;
a
sio:SIO_001121
.
}
dgn-np:NP724703.RAdpgDLdYMWYVipfg1RKcCs3LpXwOyzPpHAz0MHJj3EqU130_provenance
{
dgn-np:NP724703.RAdpgDLdYMWYVipfg1RKcCs3LpXwOyzPpHAz0MHJj3EqU130_assertion
dcterms:description
"[Renal biopsy in one consenting proband revealed significantly lower SGLT2 expression in the apical side of the proximal convoluted tubule in comparison to both healthy and disease controls (minimal change disease and diabetic nephropathy).]. 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:21165652
;
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:NP724703.RAdpgDLdYMWYVipfg1RKcCs3LpXwOyzPpHAz0MHJj3EqU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:20+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" .
}