@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP171872.RA84ykOSBgcENr4_kNMRG1IIU2gCok_8MNNMALeulYzlk
> .
@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:NP171872.RA84ykOSBgcENr4_kNMRG1IIU2gCok_8MNNMALeulYzlk130_head
{
this:
np:hasAssertion
dgn-np:NP171872.RA84ykOSBgcENr4_kNMRG1IIU2gCok_8MNNMALeulYzlk130_assertion
;
np:hasProvenance
dgn-np:NP171872.RA84ykOSBgcENr4_kNMRG1IIU2gCok_8MNNMALeulYzlk130_provenance
;
np:hasPublicationInfo
dgn-np:NP171872.RA84ykOSBgcENr4_kNMRG1IIU2gCok_8MNNMALeulYzlk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP171872.RA84ykOSBgcENr4_kNMRG1IIU2gCok_8MNNMALeulYzlk130_assertion
a
np:Assertion
.
dgn-np:NP171872.RA84ykOSBgcENr4_kNMRG1IIU2gCok_8MNNMALeulYzlk130_provenance
a
np:Provenance
.
dgn-np:NP171872.RA84ykOSBgcENr4_kNMRG1IIU2gCok_8MNNMALeulYzlk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP171872.RA84ykOSBgcENr4_kNMRG1IIU2gCok_8MNNMALeulYzlk130_assertion
{
miriam-gene:7421
a
ncit:C16612
.
lld:C0011884
a
ncit:C7057
.
dgn-gda:DGN28bc9e1073cff62de7584653425f6a8f
sio:SIO_000628
miriam-gene:7421
,
lld:C0011884
;
a
sio:SIO_001121
.
}
dgn-np:NP171872.RA84ykOSBgcENr4_kNMRG1IIU2gCok_8MNNMALeulYzlk130_provenance
{
dgn-np:NP171872.RA84ykOSBgcENr4_kNMRG1IIU2gCok_8MNNMALeulYzlk130_assertion
dcterms:description
"[In French Type I (insulin-dependent) diabetic patients, we demonstrate an association between TT form (VDR) and low risk for severe diabetic retinopathy, especially in patients with long duration, and between Tt variant and high risk for severe diabetic retinopathy in subjects with poor glycaemic control.]. 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:11914750
;
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:NP171872.RA84ykOSBgcENr4_kNMRG1IIU2gCok_8MNNMALeulYzlk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:33+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" .
}