@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP496260.RArXyKtUJ7VBQt5JDEVhGvqYsjAqAAPRPFSue6PAir_Vg
> .
@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:NP496260.RArXyKtUJ7VBQt5JDEVhGvqYsjAqAAPRPFSue6PAir_Vg130_head
{
this:
np:hasAssertion
dgn-np:NP496260.RArXyKtUJ7VBQt5JDEVhGvqYsjAqAAPRPFSue6PAir_Vg130_assertion
;
np:hasProvenance
dgn-np:NP496260.RArXyKtUJ7VBQt5JDEVhGvqYsjAqAAPRPFSue6PAir_Vg130_provenance
;
np:hasPublicationInfo
dgn-np:NP496260.RArXyKtUJ7VBQt5JDEVhGvqYsjAqAAPRPFSue6PAir_Vg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP496260.RArXyKtUJ7VBQt5JDEVhGvqYsjAqAAPRPFSue6PAir_Vg130_assertion
a
np:Assertion
.
dgn-np:NP496260.RArXyKtUJ7VBQt5JDEVhGvqYsjAqAAPRPFSue6PAir_Vg130_provenance
a
np:Provenance
.
dgn-np:NP496260.RArXyKtUJ7VBQt5JDEVhGvqYsjAqAAPRPFSue6PAir_Vg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP496260.RArXyKtUJ7VBQt5JDEVhGvqYsjAqAAPRPFSue6PAir_Vg130_assertion
{
miriam-gene:7421
a
ncit:C16612
.
lld:C0020437
a
ncit:C7057
.
dgn-gda:DGN592ddbda61f734e816c44593a2a68c2f
sio:SIO_000628
miriam-gene:7421
,
lld:C0020437
;
a
sio:SIO_001121
.
}
dgn-np:NP496260.RArXyKtUJ7VBQt5JDEVhGvqYsjAqAAPRPFSue6PAir_Vg130_provenance
{
dgn-np:NP496260.RArXyKtUJ7VBQt5JDEVhGvqYsjAqAAPRPFSue6PAir_Vg130_assertion
dcterms:description
"[Depressed PTH levels were found in sarcoidosis patients, especially in those with the bb genotype, but there was no difference in 1,25(OH)2D3 levels among the VDR genotypes, and this polymorphism also had no association with onset of hypercalcemia.]. 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:11033842
;
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:NP496260.RArXyKtUJ7VBQt5JDEVhGvqYsjAqAAPRPFSue6PAir_Vg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:56+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" .
}