@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP862954.RARdkJv1r1nu0cVK_RsHjfKWMoFrdkvv1r_3DlBh53Nms
> .
@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:NP862954.RARdkJv1r1nu0cVK_RsHjfKWMoFrdkvv1r_3DlBh53Nms130_head
{
this:
np:hasAssertion
dgn-np:NP862954.RARdkJv1r1nu0cVK_RsHjfKWMoFrdkvv1r_3DlBh53Nms130_assertion
;
np:hasProvenance
dgn-np:NP862954.RARdkJv1r1nu0cVK_RsHjfKWMoFrdkvv1r_3DlBh53Nms130_provenance
;
np:hasPublicationInfo
dgn-np:NP862954.RARdkJv1r1nu0cVK_RsHjfKWMoFrdkvv1r_3DlBh53Nms130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP862954.RARdkJv1r1nu0cVK_RsHjfKWMoFrdkvv1r_3DlBh53Nms130_assertion
a
np:Assertion
.
dgn-np:NP862954.RARdkJv1r1nu0cVK_RsHjfKWMoFrdkvv1r_3DlBh53Nms130_provenance
a
np:Provenance
.
dgn-np:NP862954.RARdkJv1r1nu0cVK_RsHjfKWMoFrdkvv1r_3DlBh53Nms130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP862954.RARdkJv1r1nu0cVK_RsHjfKWMoFrdkvv1r_3DlBh53Nms130_assertion
{
miriam-gene:3133
a
ncit:C16612
.
lld:C1609432
a
ncit:C7057
.
dgn-gda:DGN501dbb1dc643a38fd5c6ab96238198c9
sio:SIO_000628
miriam-gene:3133
,
lld:C1609432
;
a
sio:SIO_001121
.
}
dgn-np:NP862954.RARdkJv1r1nu0cVK_RsHjfKWMoFrdkvv1r_3DlBh53Nms130_provenance
{
dgn-np:NP862954.RARdkJv1r1nu0cVK_RsHjfKWMoFrdkvv1r_3DlBh53Nms130_assertion
dcterms:description
"[We show that CD is a model disease to decipher the role of MHC class II molecules in human immunopathology, to analyze the mechanisms that link tolerance to food proteins and autoimmunity, and to investigate how chronic activation of IEL can lead to T cell lymphomagenesis.]. 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:22749351
;
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:NP862954.RARdkJv1r1nu0cVK_RsHjfKWMoFrdkvv1r_3DlBh53Nms130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:47+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" .
}