@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP689732.RA2On26fyNnhPRwKETMAKb8md29Aw1Y7EWvUZLIbYpKZs
> .
@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:NP689732.RA2On26fyNnhPRwKETMAKb8md29Aw1Y7EWvUZLIbYpKZs130_head
{
this:
np:hasAssertion
dgn-np:NP689732.RA2On26fyNnhPRwKETMAKb8md29Aw1Y7EWvUZLIbYpKZs130_assertion
;
np:hasProvenance
dgn-np:NP689732.RA2On26fyNnhPRwKETMAKb8md29Aw1Y7EWvUZLIbYpKZs130_provenance
;
np:hasPublicationInfo
dgn-np:NP689732.RA2On26fyNnhPRwKETMAKb8md29Aw1Y7EWvUZLIbYpKZs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP689732.RA2On26fyNnhPRwKETMAKb8md29Aw1Y7EWvUZLIbYpKZs130_assertion
a
np:Assertion
.
dgn-np:NP689732.RA2On26fyNnhPRwKETMAKb8md29Aw1Y7EWvUZLIbYpKZs130_provenance
a
np:Provenance
.
dgn-np:NP689732.RA2On26fyNnhPRwKETMAKb8md29Aw1Y7EWvUZLIbYpKZs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP689732.RA2On26fyNnhPRwKETMAKb8md29Aw1Y7EWvUZLIbYpKZs130_assertion
{
miriam-gene:920
a
ncit:C16612
.
lld:C0021053
a
ncit:C7057
.
dgn-gda:DGNfc89266386c5beb4f4d0646e2852dd31
sio:SIO_000628
miriam-gene:920
,
lld:C0021053
;
a
sio:SIO_001121
.
}
dgn-np:NP689732.RA2On26fyNnhPRwKETMAKb8md29Aw1Y7EWvUZLIbYpKZs130_provenance
{
dgn-np:NP689732.RA2On26fyNnhPRwKETMAKb8md29Aw1Y7EWvUZLIbYpKZs130_assertion
dcterms:description
"[Genetic data, among others, suggest that viral infections are implicated and that natural killer effector pathways are important in the pathogenesis of CD, but most prominently these data converge with existing immunological findings that CD is primarily a T cell-mediated immune disorder in which CD4(+) T cells that recognize gluten peptides in the context of major histocompatibility class II molecules play a central role.]. 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:21219178
;
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:NP689732.RA2On26fyNnhPRwKETMAKb8md29Aw1Y7EWvUZLIbYpKZs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:59+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" .
}