@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP497637.RAQnVqXv43A-PA6CxpiUCBQVOJCxVVjpjhs3s2Mtk7KAU
> .
@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:NP497637.RAQnVqXv43A-PA6CxpiUCBQVOJCxVVjpjhs3s2Mtk7KAU130_head
{
this:
np:hasAssertion
dgn-np:NP497637.RAQnVqXv43A-PA6CxpiUCBQVOJCxVVjpjhs3s2Mtk7KAU130_assertion
;
np:hasProvenance
dgn-np:NP497637.RAQnVqXv43A-PA6CxpiUCBQVOJCxVVjpjhs3s2Mtk7KAU130_provenance
;
np:hasPublicationInfo
dgn-np:NP497637.RAQnVqXv43A-PA6CxpiUCBQVOJCxVVjpjhs3s2Mtk7KAU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP497637.RAQnVqXv43A-PA6CxpiUCBQVOJCxVVjpjhs3s2Mtk7KAU130_assertion
a
np:Assertion
.
dgn-np:NP497637.RAQnVqXv43A-PA6CxpiUCBQVOJCxVVjpjhs3s2Mtk7KAU130_provenance
a
np:Provenance
.
dgn-np:NP497637.RAQnVqXv43A-PA6CxpiUCBQVOJCxVVjpjhs3s2Mtk7KAU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP497637.RAQnVqXv43A-PA6CxpiUCBQVOJCxVVjpjhs3s2Mtk7KAU130_assertion
{
miriam-gene:1756
a
ncit:C16612
.
lld:C0001622
a
ncit:C7057
.
dgn-gda:DGNc0084149f4412a331ea9032d5774419c
sio:SIO_000628
miriam-gene:1756
,
lld:C0001622
;
a
sio:SIO_001121
.
}
dgn-np:NP497637.RAQnVqXv43A-PA6CxpiUCBQVOJCxVVjpjhs3s2Mtk7KAU130_provenance
{
dgn-np:NP497637.RAQnVqXv43A-PA6CxpiUCBQVOJCxVVjpjhs3s2Mtk7KAU130_assertion
dcterms:description
"[The data showed lack of association between BMD and these widely studied VDR polymorphisms, suggesting that the effect of endogenous hypercortisolism on bone in the context of CD does not depend on VDR genotypes.]. 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:22570981
;
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:NP497637.RAQnVqXv43A-PA6CxpiUCBQVOJCxVVjpjhs3s2Mtk7KAU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:57+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" .
}