@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP295306.RAz26up_0zahG1dxCM6yKtXrEe0LCm5DRZPBG53G01tWo
> .
@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:NP295306.RAz26up_0zahG1dxCM6yKtXrEe0LCm5DRZPBG53G01tWo130_head
{
this:
np:hasAssertion
dgn-np:NP295306.RAz26up_0zahG1dxCM6yKtXrEe0LCm5DRZPBG53G01tWo130_assertion
;
np:hasProvenance
dgn-np:NP295306.RAz26up_0zahG1dxCM6yKtXrEe0LCm5DRZPBG53G01tWo130_provenance
;
np:hasPublicationInfo
dgn-np:NP295306.RAz26up_0zahG1dxCM6yKtXrEe0LCm5DRZPBG53G01tWo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP295306.RAz26up_0zahG1dxCM6yKtXrEe0LCm5DRZPBG53G01tWo130_assertion
a
np:Assertion
.
dgn-np:NP295306.RAz26up_0zahG1dxCM6yKtXrEe0LCm5DRZPBG53G01tWo130_provenance
a
np:Provenance
.
dgn-np:NP295306.RAz26up_0zahG1dxCM6yKtXrEe0LCm5DRZPBG53G01tWo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP295306.RAz26up_0zahG1dxCM6yKtXrEe0LCm5DRZPBG53G01tWo130_assertion
{
miriam-gene:7421
a
ncit:C16612
.
lld:C2316810
a
ncit:C7057
.
dgn-gda:DGNbbc339761ba57de786a0b392ee5848ea
sio:SIO_000628
miriam-gene:7421
,
lld:C2316810
;
a
sio:SIO_001121
.
}
dgn-np:NP295306.RAz26up_0zahG1dxCM6yKtXrEe0LCm5DRZPBG53G01tWo130_provenance
{
dgn-np:NP295306.RAz26up_0zahG1dxCM6yKtXrEe0LCm5DRZPBG53G01tWo130_assertion
dcterms:description
"[No significant differences were observed in genotype or allele frequencies between case and control groups for VDR, CYP27B1 or CYP2R1 SNPs, either before or after stratification by recruitment centre or when restricted to patients with end-stage renal disease.]. 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:19783860
;
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:NP295306.RAz26up_0zahG1dxCM6yKtXrEe0LCm5DRZPBG53G01tWo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:48+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" .
}