@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP850232.RALA2Gq5zfxTjPHetn-IzWXld17clktGf6GdrdA5odq5w
> .
@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:NP850232.RALA2Gq5zfxTjPHetn-IzWXld17clktGf6GdrdA5odq5w130_head
{
this:
np:hasAssertion
dgn-np:NP850232.RALA2Gq5zfxTjPHetn-IzWXld17clktGf6GdrdA5odq5w130_assertion
;
np:hasProvenance
dgn-np:NP850232.RALA2Gq5zfxTjPHetn-IzWXld17clktGf6GdrdA5odq5w130_provenance
;
np:hasPublicationInfo
dgn-np:NP850232.RALA2Gq5zfxTjPHetn-IzWXld17clktGf6GdrdA5odq5w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP850232.RALA2Gq5zfxTjPHetn-IzWXld17clktGf6GdrdA5odq5w130_assertion
a
np:Assertion
.
dgn-np:NP850232.RALA2Gq5zfxTjPHetn-IzWXld17clktGf6GdrdA5odq5w130_provenance
a
np:Provenance
.
dgn-np:NP850232.RALA2Gq5zfxTjPHetn-IzWXld17clktGf6GdrdA5odq5w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP850232.RALA2Gq5zfxTjPHetn-IzWXld17clktGf6GdrdA5odq5w130_assertion
{
miriam-gene:1628
a
ncit:C16612
.
lld:C0026769
a
ncit:C7057
.
dgn-gda:DGNc4f59fce0c6f3283db6ee762a3ca5652
sio:SIO_000628
miriam-gene:1628
,
lld:C0026769
;
a
sio:SIO_001121
.
}
dgn-np:NP850232.RALA2Gq5zfxTjPHetn-IzWXld17clktGf6GdrdA5odq5w130_provenance
{
dgn-np:NP850232.RALA2Gq5zfxTjPHetn-IzWXld17clktGf6GdrdA5odq5w130_assertion
dcterms:description
"[The objective of this study was to determine whether polymorphisms in VDR, CYP27B1, CYP24A1, CYP2R1 and DBP are associated with the risk of MS and whether these variants may modify associations between environmental or dietary vitamin D on MS risk.]. 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:20007432
;
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:NP850232.RALA2Gq5zfxTjPHetn-IzWXld17clktGf6GdrdA5odq5w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:39+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" .
}