@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP437527.RAdvof2EZIuTgpFJo6BYaRYN8NHXYNrT0CWoQjGUUofd0
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP437527.RAdvof2EZIuTgpFJo6BYaRYN8NHXYNrT0CWoQjGUUofd0130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP437527.RAdvof2EZIuTgpFJo6BYaRYN8NHXYNrT0CWoQjGUUofd0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP437527.RAdvof2EZIuTgpFJo6BYaRYN8NHXYNrT0CWoQjGUUofd0130_assertion
a
np:Assertion
.
dgn-np:NP437527.RAdvof2EZIuTgpFJo6BYaRYN8NHXYNrT0CWoQjGUUofd0130_provenance
a
np:Provenance
.
dgn-np:NP437527.RAdvof2EZIuTgpFJo6BYaRYN8NHXYNrT0CWoQjGUUofd0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP437527.RAdvof2EZIuTgpFJo6BYaRYN8NHXYNrT0CWoQjGUUofd0130_assertion
{
miriam-gene:1594
a
ncit:C16612
.
lld:C0011884
a
ncit:C7057
.
dgn-gda:DGN6b882356557c515aaf31591b646890b8
sio:SIO_000628
miriam-gene:1594
,
lld:C0011884
;
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sio:SIO_001121
.
}
dgn-np:NP437527.RAdvof2EZIuTgpFJo6BYaRYN8NHXYNrT0CWoQjGUUofd0130_provenance
{
dgn-np:NP437527.RAdvof2EZIuTgpFJo6BYaRYN8NHXYNrT0CWoQjGUUofd0130_assertion
dcterms:description
"[After correcting for duration of disease, only the VDR gene BsmI genotypes showed significant association with cumulative prevalence of diabetic retinopathy, while no investigated genetic polymorphysms could reliably predict 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:20120526
;
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 .
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dgn-np:NP437527.RAdvof2EZIuTgpFJo6BYaRYN8NHXYNrT0CWoQjGUUofd0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:19+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" .
}