@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP63330.RAx1eAyf3VjBGWY_dfBP7xxO21sxrTeXUlNeP45IQY0dk
> .
@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:NP63330.RAx1eAyf3VjBGWY_dfBP7xxO21sxrTeXUlNeP45IQY0dk130_head
{
this:
np:hasAssertion
dgn-np:NP63330.RAx1eAyf3VjBGWY_dfBP7xxO21sxrTeXUlNeP45IQY0dk130_assertion
;
np:hasProvenance
dgn-np:NP63330.RAx1eAyf3VjBGWY_dfBP7xxO21sxrTeXUlNeP45IQY0dk130_provenance
;
np:hasPublicationInfo
dgn-np:NP63330.RAx1eAyf3VjBGWY_dfBP7xxO21sxrTeXUlNeP45IQY0dk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP63330.RAx1eAyf3VjBGWY_dfBP7xxO21sxrTeXUlNeP45IQY0dk130_assertion
a
np:Assertion
.
dgn-np:NP63330.RAx1eAyf3VjBGWY_dfBP7xxO21sxrTeXUlNeP45IQY0dk130_provenance
a
np:Provenance
.
dgn-np:NP63330.RAx1eAyf3VjBGWY_dfBP7xxO21sxrTeXUlNeP45IQY0dk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP63330.RAx1eAyf3VjBGWY_dfBP7xxO21sxrTeXUlNeP45IQY0dk130_assertion
{
miriam-gene:7133
a
ncit:C16612
.
lld:C0042164
a
ncit:C7057
.
dgn-gda:DGN78a1cbdf4d51e8a1a587562c468c3eb9
sio:SIO_000628
miriam-gene:7133
,
lld:C0042164
;
a
sio:SIO_001122
.
}
dgn-np:NP63330.RAx1eAyf3VjBGWY_dfBP7xxO21sxrTeXUlNeP45IQY0dk130_provenance
{
dgn-np:NP63330.RAx1eAyf3VjBGWY_dfBP7xxO21sxrTeXUlNeP45IQY0dk130_assertion
dcterms:description
"[ A significant difference in the frequency of TNF-857T allele was found in patients with IAU. There was a trend toward the development of inflammation-related complications in HLA-B27(+) patients with IAU who were carriers of TNFRSF1A-201T or TNFRSF1A-1135T alleles. Genetic variations in these proinflammatory mediators and their receptors appear to influence the susceptibility and severity of the inflammatory response within the eyes of patients during the development of IAU.]. 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:15851552
;
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:NP63330.RAx1eAyf3VjBGWY_dfBP7xxO21sxrTeXUlNeP45IQY0dk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:30+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" .
}