@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP522501.RANzcRIJgkAKEr7nbbCZ3GY0pkhUlIbl-Aq7CuyCcE2ro
> .
@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:NP522501.RANzcRIJgkAKEr7nbbCZ3GY0pkhUlIbl-Aq7CuyCcE2ro130_head
{
this:
np:hasAssertion
dgn-np:NP522501.RANzcRIJgkAKEr7nbbCZ3GY0pkhUlIbl-Aq7CuyCcE2ro130_assertion
;
np:hasProvenance
dgn-np:NP522501.RANzcRIJgkAKEr7nbbCZ3GY0pkhUlIbl-Aq7CuyCcE2ro130_provenance
;
np:hasPublicationInfo
dgn-np:NP522501.RANzcRIJgkAKEr7nbbCZ3GY0pkhUlIbl-Aq7CuyCcE2ro130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP522501.RANzcRIJgkAKEr7nbbCZ3GY0pkhUlIbl-Aq7CuyCcE2ro130_assertion
a
np:Assertion
.
dgn-np:NP522501.RANzcRIJgkAKEr7nbbCZ3GY0pkhUlIbl-Aq7CuyCcE2ro130_provenance
a
np:Provenance
.
dgn-np:NP522501.RANzcRIJgkAKEr7nbbCZ3GY0pkhUlIbl-Aq7CuyCcE2ro130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP522501.RANzcRIJgkAKEr7nbbCZ3GY0pkhUlIbl-Aq7CuyCcE2ro130_assertion
{
miriam-gene:1594
a
ncit:C16612
.
lld:C0342922
a
ncit:C7057
.
dgn-gda:DGN5021c4d740297858b26ce912b124fdc7
sio:SIO_000628
miriam-gene:1594
,
lld:C0342922
;
a
sio:SIO_001121
.
}
dgn-np:NP522501.RANzcRIJgkAKEr7nbbCZ3GY0pkhUlIbl-Aq7CuyCcE2ro130_provenance
{
dgn-np:NP522501.RANzcRIJgkAKEr7nbbCZ3GY0pkhUlIbl-Aq7CuyCcE2ro130_assertion
dcterms:description
"[Although it is not clear why a presumed better-functioning VDR variant (F allele) is associated with an increased risk of developing rickets, this study raises the possibility that VDR alleles might be important in determining an individual's susceptibility to developing rickets when faced with dietary calcium deficiency.]. 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:11092401
;
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:NP522501.RANzcRIJgkAKEr7nbbCZ3GY0pkhUlIbl-Aq7CuyCcE2ro130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:11+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" .
}