@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP345781.RALru7B0FqlgM7_yq1TfK1Z39xdE3HaOphG_miYpRQxsk
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP345781.RALru7B0FqlgM7_yq1TfK1Z39xdE3HaOphG_miYpRQxsk130_head
{
this:
np:hasAssertion
dgn-np:NP345781.RALru7B0FqlgM7_yq1TfK1Z39xdE3HaOphG_miYpRQxsk130_assertion
;
np:hasProvenance
dgn-np:NP345781.RALru7B0FqlgM7_yq1TfK1Z39xdE3HaOphG_miYpRQxsk130_provenance
;
np:hasPublicationInfo
dgn-np:NP345781.RALru7B0FqlgM7_yq1TfK1Z39xdE3HaOphG_miYpRQxsk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP345781.RALru7B0FqlgM7_yq1TfK1Z39xdE3HaOphG_miYpRQxsk130_assertion
a
np:Assertion
.
dgn-np:NP345781.RALru7B0FqlgM7_yq1TfK1Z39xdE3HaOphG_miYpRQxsk130_provenance
a
np:Provenance
.
dgn-np:NP345781.RALru7B0FqlgM7_yq1TfK1Z39xdE3HaOphG_miYpRQxsk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP345781.RALru7B0FqlgM7_yq1TfK1Z39xdE3HaOphG_miYpRQxsk130_assertion
{
miriam-gene:1594
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN13dfd9e0c4d4e9c0297aa78fd65ce8d3
sio:SIO_000628
miriam-gene:1594
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP345781.RALru7B0FqlgM7_yq1TfK1Z39xdE3HaOphG_miYpRQxsk130_provenance
{
dgn-np:NP345781.RALru7B0FqlgM7_yq1TfK1Z39xdE3HaOphG_miYpRQxsk130_assertion
dcterms:description
"[To conclude, there is some indication that VDR polymorphisms may modulate the risk of some cancer sites and in future studies VDR genetic variation should be integrated also with prediagnostic indicator of vitamin D status.]. 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:25207361
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP345781.RALru7B0FqlgM7_yq1TfK1Z39xdE3HaOphG_miYpRQxsk130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:40:59+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}