@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP480369.RA43Yi0s99FTanacUSgXeOKrlD_prZr-GF_RJAuI7W_bY
> .
@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:NP480369.RA43Yi0s99FTanacUSgXeOKrlD_prZr-GF_RJAuI7W_bY130_head
{
this:
np:hasAssertion
dgn-np:NP480369.RA43Yi0s99FTanacUSgXeOKrlD_prZr-GF_RJAuI7W_bY130_assertion
;
np:hasProvenance
dgn-np:NP480369.RA43Yi0s99FTanacUSgXeOKrlD_prZr-GF_RJAuI7W_bY130_provenance
;
np:hasPublicationInfo
dgn-np:NP480369.RA43Yi0s99FTanacUSgXeOKrlD_prZr-GF_RJAuI7W_bY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP480369.RA43Yi0s99FTanacUSgXeOKrlD_prZr-GF_RJAuI7W_bY130_assertion
a
np:Assertion
.
dgn-np:NP480369.RA43Yi0s99FTanacUSgXeOKrlD_prZr-GF_RJAuI7W_bY130_provenance
a
np:Provenance
.
dgn-np:NP480369.RA43Yi0s99FTanacUSgXeOKrlD_prZr-GF_RJAuI7W_bY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP480369.RA43Yi0s99FTanacUSgXeOKrlD_prZr-GF_RJAuI7W_bY130_assertion
{
miriam-gene:100271696
a
ncit:C16612
.
lld:C0026769
a
ncit:C7057
.
dgn-gda:DGN45d7ef74844d6c38d005aa58101e2a65
sio:SIO_000628
miriam-gene:100271696
,
lld:C0026769
;
a
sio:SIO_001121
.
}
dgn-np:NP480369.RA43Yi0s99FTanacUSgXeOKrlD_prZr-GF_RJAuI7W_bY130_provenance
{
dgn-np:NP480369.RA43Yi0s99FTanacUSgXeOKrlD_prZr-GF_RJAuI7W_bY130_assertion
dcterms:description
"[VDR rs2228570 and rs731236 allelic and genotype frequencies did not differ significantly between MS patients and controls, and were unrelated with the age of onset of MS, gender, and course of MS. HLADRB1*1501 showed a high association with the risk of developing MS 4.76(95% C.I.]. 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:23840333
;
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:NP480369.RA43Yi0s99FTanacUSgXeOKrlD_prZr-GF_RJAuI7W_bY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:47+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" .
}