@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP800164.RAiBd5tSRm1KWBgdqk0SKUbN42LWIsgvHG2BmEojEAY50
> .
@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:NP800164.RAiBd5tSRm1KWBgdqk0SKUbN42LWIsgvHG2BmEojEAY50130_head
{
this:
np:hasAssertion
dgn-np:NP800164.RAiBd5tSRm1KWBgdqk0SKUbN42LWIsgvHG2BmEojEAY50130_assertion
;
np:hasProvenance
dgn-np:NP800164.RAiBd5tSRm1KWBgdqk0SKUbN42LWIsgvHG2BmEojEAY50130_provenance
;
np:hasPublicationInfo
dgn-np:NP800164.RAiBd5tSRm1KWBgdqk0SKUbN42LWIsgvHG2BmEojEAY50130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP800164.RAiBd5tSRm1KWBgdqk0SKUbN42LWIsgvHG2BmEojEAY50130_assertion
a
np:Assertion
.
dgn-np:NP800164.RAiBd5tSRm1KWBgdqk0SKUbN42LWIsgvHG2BmEojEAY50130_provenance
a
np:Provenance
.
dgn-np:NP800164.RAiBd5tSRm1KWBgdqk0SKUbN42LWIsgvHG2BmEojEAY50130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP800164.RAiBd5tSRm1KWBgdqk0SKUbN42LWIsgvHG2BmEojEAY50130_assertion
{
miriam-gene:846
a
ncit:C16612
.
lld:C0392525
a
ncit:C7057
.
dgn-gda:DGN0cf6b06dd115bf6501c05b656ecab147
sio:SIO_000628
miriam-gene:846
,
lld:C0392525
;
a
sio:SIO_001121
.
}
dgn-np:NP800164.RAiBd5tSRm1KWBgdqk0SKUbN42LWIsgvHG2BmEojEAY50130_provenance
{
dgn-np:NP800164.RAiBd5tSRm1KWBgdqk0SKUbN42LWIsgvHG2BmEojEAY50130_assertion
dcterms:description
"[Bioinformatic analysis suggested that the minor alleles at these polymorphisms were able to modify the binding sites of specific transcription factors and, consequently, CaSR expression.Our studies suggest that CaSR is one of the candidate genes explaining individual predisposition to calcium nephrolithiasis.]. 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:22107799
;
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:NP800164.RAiBd5tSRm1KWBgdqk0SKUbN42LWIsgvHG2BmEojEAY50130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:11+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" .
}