@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP995174.RA5kekIiA639ksHGEu2Rd1aa-z_ahtqTr2qV2de6rpBTk
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP995174.RA5kekIiA639ksHGEu2Rd1aa-z_ahtqTr2qV2de6rpBTk130_head
{
this:
np:hasAssertion
dgn-np:NP995174.RA5kekIiA639ksHGEu2Rd1aa-z_ahtqTr2qV2de6rpBTk130_assertion
;
np:hasProvenance
dgn-np:NP995174.RA5kekIiA639ksHGEu2Rd1aa-z_ahtqTr2qV2de6rpBTk130_provenance
;
np:hasPublicationInfo
dgn-np:NP995174.RA5kekIiA639ksHGEu2Rd1aa-z_ahtqTr2qV2de6rpBTk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP995174.RA5kekIiA639ksHGEu2Rd1aa-z_ahtqTr2qV2de6rpBTk130_assertion
a
np:Assertion
.
dgn-np:NP995174.RA5kekIiA639ksHGEu2Rd1aa-z_ahtqTr2qV2de6rpBTk130_provenance
a
np:Provenance
.
dgn-np:NP995174.RA5kekIiA639ksHGEu2Rd1aa-z_ahtqTr2qV2de6rpBTk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP995174.RA5kekIiA639ksHGEu2Rd1aa-z_ahtqTr2qV2de6rpBTk130_assertion
{
miriam-gene:7421
a
ncit:C16612
.
lld:C0042900
a
ncit:C7057
.
dgn-gda:DGN82ca4ef7a1470ae48f02a95a8af91848
sio:SIO_000628
miriam-gene:7421
,
lld:C0042900
;
a
sio:SIO_001121
.
}
dgn-np:NP995174.RA5kekIiA639ksHGEu2Rd1aa-z_ahtqTr2qV2de6rpBTk130_provenance
{
dgn-np:NP995174.RA5kekIiA639ksHGEu2Rd1aa-z_ahtqTr2qV2de6rpBTk130_assertion
dcterms:description
"[Genetic variations within the vitamin D receptor (VDR) gene could lead to significant receptor dysfunction, and could further affect the formation of the biologically active 25(OH)D. Therefore, we hypothesized that VDR polymorphisms might be involved in vitiligo by affecting the formation of 25(OH)D.]. 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:22762534
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP995174.RA5kekIiA639ksHGEu2Rd1aa-z_ahtqTr2qV2de6rpBTk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:16+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}