@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP46645.RAQbRKatvwinaWbafgf1F0v9BzCxC0k35xZM2ThQ4d6AI
> .
@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:NP46645.RAQbRKatvwinaWbafgf1F0v9BzCxC0k35xZM2ThQ4d6AI130_head
{
this:
np:hasAssertion
dgn-np:NP46645.RAQbRKatvwinaWbafgf1F0v9BzCxC0k35xZM2ThQ4d6AI130_assertion
;
np:hasProvenance
dgn-np:NP46645.RAQbRKatvwinaWbafgf1F0v9BzCxC0k35xZM2ThQ4d6AI130_provenance
;
np:hasPublicationInfo
dgn-np:NP46645.RAQbRKatvwinaWbafgf1F0v9BzCxC0k35xZM2ThQ4d6AI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP46645.RAQbRKatvwinaWbafgf1F0v9BzCxC0k35xZM2ThQ4d6AI130_assertion
a
np:Assertion
.
dgn-np:NP46645.RAQbRKatvwinaWbafgf1F0v9BzCxC0k35xZM2ThQ4d6AI130_provenance
a
np:Provenance
.
dgn-np:NP46645.RAQbRKatvwinaWbafgf1F0v9BzCxC0k35xZM2ThQ4d6AI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP46645.RAQbRKatvwinaWbafgf1F0v9BzCxC0k35xZM2ThQ4d6AI130_assertion
{
miriam-gene:1298
a
ncit:C16612
.
lld:C0158266
a
ncit:C7057
.
dgn-gda:DGNe0e779ce79a4a4b7d97edc15c8d66015
sio:SIO_000628
miriam-gene:1298
,
lld:C0158266
;
a
sio:SIO_001122
.
}
dgn-np:NP46645.RAQbRKatvwinaWbafgf1F0v9BzCxC0k35xZM2ThQ4d6AI130_provenance
{
dgn-np:NP46645.RAQbRKatvwinaWbafgf1F0v9BzCxC0k35xZM2ThQ4d6AI130_assertion
dcterms:description
"[ This largest-ever population study using MRI to define DDD demonstrates for the first time that the Trp2 allele is a significant risk factor for the development and severity of degeneration. The association is age- dependent as it is more prevalent in some age groups than in others. The contrasting Trp allele frequencies between the Finns and the Chinese are the first indication that the genetic risk factors for DDD varies between ethnic groups.]. 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:16371896
;
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:NP46645.RAQbRKatvwinaWbafgf1F0v9BzCxC0k35xZM2ThQ4d6AI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:21+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" .
}