@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP450229.RAO1G_Slg3AycY3hd33q9h064D4LyHB_pmFJWDsRWspJQ
> .
@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:NP450229.RAO1G_Slg3AycY3hd33q9h064D4LyHB_pmFJWDsRWspJQ130_head
{
this:
np:hasAssertion
dgn-np:NP450229.RAO1G_Slg3AycY3hd33q9h064D4LyHB_pmFJWDsRWspJQ130_assertion
;
np:hasProvenance
dgn-np:NP450229.RAO1G_Slg3AycY3hd33q9h064D4LyHB_pmFJWDsRWspJQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP450229.RAO1G_Slg3AycY3hd33q9h064D4LyHB_pmFJWDsRWspJQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP450229.RAO1G_Slg3AycY3hd33q9h064D4LyHB_pmFJWDsRWspJQ130_assertion
a
np:Assertion
.
dgn-np:NP450229.RAO1G_Slg3AycY3hd33q9h064D4LyHB_pmFJWDsRWspJQ130_provenance
a
np:Provenance
.
dgn-np:NP450229.RAO1G_Slg3AycY3hd33q9h064D4LyHB_pmFJWDsRWspJQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP450229.RAO1G_Slg3AycY3hd33q9h064D4LyHB_pmFJWDsRWspJQ130_assertion
{
miriam-gene:3133
a
ncit:C16612
.
lld:C0242583
a
ncit:C7057
.
dgn-gda:DGN9d2258348cf3589a7fc01059f23e3383
sio:SIO_000628
miriam-gene:3133
,
lld:C0242583
;
a
sio:SIO_001121
.
}
dgn-np:NP450229.RAO1G_Slg3AycY3hd33q9h064D4LyHB_pmFJWDsRWspJQ130_provenance
{
dgn-np:NP450229.RAO1G_Slg3AycY3hd33q9h064D4LyHB_pmFJWDsRWspJQ130_assertion
dcterms:description
"[Because of the central role the class II MHC molecules play in immune system function, it is not surprising that the lack of expression of these molecules results in a severe combined immunodeficiency disorder (called bare lymphocyte syndrome) and that the aberrant expression of the molecules is frequently observed in the target organs of various autoimmune disorders (e.g., multiple sclerosis and rheumatoid arthritis).]. 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:7589984
;
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:NP450229.RAO1G_Slg3AycY3hd33q9h064D4LyHB_pmFJWDsRWspJQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:28+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" .
}