@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP353956.RAyTJiixyer7GfoNCbiXzTUvvjsT0iJghhdyejLzEVRnM
> .
@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:NP353956.RAyTJiixyer7GfoNCbiXzTUvvjsT0iJghhdyejLzEVRnM130_head
{
this:
np:hasAssertion
dgn-np:NP353956.RAyTJiixyer7GfoNCbiXzTUvvjsT0iJghhdyejLzEVRnM130_assertion
;
np:hasProvenance
dgn-np:NP353956.RAyTJiixyer7GfoNCbiXzTUvvjsT0iJghhdyejLzEVRnM130_provenance
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np:hasPublicationInfo
dgn-np:NP353956.RAyTJiixyer7GfoNCbiXzTUvvjsT0iJghhdyejLzEVRnM130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP353956.RAyTJiixyer7GfoNCbiXzTUvvjsT0iJghhdyejLzEVRnM130_assertion
a
np:Assertion
.
dgn-np:NP353956.RAyTJiixyer7GfoNCbiXzTUvvjsT0iJghhdyejLzEVRnM130_provenance
a
np:Provenance
.
dgn-np:NP353956.RAyTJiixyer7GfoNCbiXzTUvvjsT0iJghhdyejLzEVRnM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP353956.RAyTJiixyer7GfoNCbiXzTUvvjsT0iJghhdyejLzEVRnM130_assertion
{
miriam-gene:2837
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGN45f9ced83d1ed1f2f9df76f27e57bbd7
sio:SIO_000628
miriam-gene:2837
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP353956.RAyTJiixyer7GfoNCbiXzTUvvjsT0iJghhdyejLzEVRnM130_provenance
{
dgn-np:NP353956.RAyTJiixyer7GfoNCbiXzTUvvjsT0iJghhdyejLzEVRnM130_assertion
dcterms:description
"[Five polymorphic variants of the VDR gene, including Cdx-2 (intron 1e) and FokI (exon 2) present in the 5' region of the gene, and BsmI (intron 8), ApaI (intron 8), and TaqI (exon 9) sites present in the 3' untranslated region (UTR), were evaluated for possible associations with colorectal cancer risk.]. 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:22529698
;
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:NP353956.RAyTJiixyer7GfoNCbiXzTUvvjsT0iJghhdyejLzEVRnM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:27+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" .
}