@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP236760.RA2HXN-LWzrcSvAbunhTebK4hUz6z-QA__9ljleYVk4S8
> .
@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:NP236760.RA2HXN-LWzrcSvAbunhTebK4hUz6z-QA__9ljleYVk4S8130_head
{
this:
np:hasAssertion
dgn-np:NP236760.RA2HXN-LWzrcSvAbunhTebK4hUz6z-QA__9ljleYVk4S8130_assertion
;
np:hasProvenance
dgn-np:NP236760.RA2HXN-LWzrcSvAbunhTebK4hUz6z-QA__9ljleYVk4S8130_provenance
;
np:hasPublicationInfo
dgn-np:NP236760.RA2HXN-LWzrcSvAbunhTebK4hUz6z-QA__9ljleYVk4S8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP236760.RA2HXN-LWzrcSvAbunhTebK4hUz6z-QA__9ljleYVk4S8130_assertion
a
np:Assertion
.
dgn-np:NP236760.RA2HXN-LWzrcSvAbunhTebK4hUz6z-QA__9ljleYVk4S8130_provenance
a
np:Provenance
.
dgn-np:NP236760.RA2HXN-LWzrcSvAbunhTebK4hUz6z-QA__9ljleYVk4S8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP236760.RA2HXN-LWzrcSvAbunhTebK4hUz6z-QA__9ljleYVk4S8130_assertion
{
miriam-gene:1493
a
ncit:C16612
.
lld:C0178468
a
ncit:C7057
.
dgn-gda:DGN73ab4f1a9f5e219290d6e1c24346e9d7
sio:SIO_000628
miriam-gene:1493
,
lld:C0178468
;
a
sio:SIO_001121
.
}
dgn-np:NP236760.RA2HXN-LWzrcSvAbunhTebK4hUz6z-QA__9ljleYVk4S8130_provenance
{
dgn-np:NP236760.RA2HXN-LWzrcSvAbunhTebK4hUz6z-QA__9ljleYVk4S8130_assertion
dcterms:description
"[Due to the functional relevance of the Fas pathway in autoimmune thyroid disease we were interested in the possible contribution of polymorphisms in the Fas gene to the genetic risk of thyroid autoimmunity, which so far is mainly, but incompletely, attributed to the HLA DQ region and polymorphisms in the CTLA-4 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:14585083
;
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:NP236760.RA2HXN-LWzrcSvAbunhTebK4hUz6z-QA__9ljleYVk4S8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:12+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" .
}