@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP62574.RA-QMryKRxJpnVIE4fC14OGLT2YLcem0OD6rhDRc2XRNk
> .
@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:NP62574.RA-QMryKRxJpnVIE4fC14OGLT2YLcem0OD6rhDRc2XRNk130_head
{
this:
np:hasAssertion
dgn-np:NP62574.RA-QMryKRxJpnVIE4fC14OGLT2YLcem0OD6rhDRc2XRNk130_assertion
;
np:hasProvenance
dgn-np:NP62574.RA-QMryKRxJpnVIE4fC14OGLT2YLcem0OD6rhDRc2XRNk130_provenance
;
np:hasPublicationInfo
dgn-np:NP62574.RA-QMryKRxJpnVIE4fC14OGLT2YLcem0OD6rhDRc2XRNk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP62574.RA-QMryKRxJpnVIE4fC14OGLT2YLcem0OD6rhDRc2XRNk130_assertion
a
np:Assertion
.
dgn-np:NP62574.RA-QMryKRxJpnVIE4fC14OGLT2YLcem0OD6rhDRc2XRNk130_provenance
a
np:Provenance
.
dgn-np:NP62574.RA-QMryKRxJpnVIE4fC14OGLT2YLcem0OD6rhDRc2XRNk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP62574.RA-QMryKRxJpnVIE4fC14OGLT2YLcem0OD6rhDRc2XRNk130_assertion
{
miriam-gene:7421
a
ncit:C16612
.
lld:C0221775
a
ncit:C7057
.
dgn-gda:DGN614c7849978f4643c849de66efef1ab4
sio:SIO_000628
miriam-gene:7421
,
lld:C0221775
;
a
sio:SIO_001122
.
}
dgn-np:NP62574.RA-QMryKRxJpnVIE4fC14OGLT2YLcem0OD6rhDRc2XRNk130_provenance
{
dgn-np:NP62574.RA-QMryKRxJpnVIE4fC14OGLT2YLcem0OD6rhDRc2XRNk130_assertion
dcterms:description
"[ This study revealed that the Tt allele of the vitamin-D receptor gene was more frequently associated with multilevel and severe disc degeneration and disc herniation than was the TT allele, pointing to an increased risk of disc disease at an early age in subjects with the Tt allele in the vitamin-D receptor gene.]. 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:12429765
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP62574.RA-QMryKRxJpnVIE4fC14OGLT2YLcem0OD6rhDRc2XRNk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:29+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" .
}