@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP336579.RAJ7z9Z-Zon-9e0UlL2so7oppqicReU3on1tnC79CZKoU
> .
@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:NP336579.RAJ7z9Z-Zon-9e0UlL2so7oppqicReU3on1tnC79CZKoU130_head
{
this:
np:hasAssertion
dgn-np:NP336579.RAJ7z9Z-Zon-9e0UlL2so7oppqicReU3on1tnC79CZKoU130_assertion
;
np:hasProvenance
dgn-np:NP336579.RAJ7z9Z-Zon-9e0UlL2so7oppqicReU3on1tnC79CZKoU130_provenance
;
np:hasPublicationInfo
dgn-np:NP336579.RAJ7z9Z-Zon-9e0UlL2so7oppqicReU3on1tnC79CZKoU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP336579.RAJ7z9Z-Zon-9e0UlL2so7oppqicReU3on1tnC79CZKoU130_assertion
a
np:Assertion
.
dgn-np:NP336579.RAJ7z9Z-Zon-9e0UlL2so7oppqicReU3on1tnC79CZKoU130_provenance
a
np:Provenance
.
dgn-np:NP336579.RAJ7z9Z-Zon-9e0UlL2so7oppqicReU3on1tnC79CZKoU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP336579.RAJ7z9Z-Zon-9e0UlL2so7oppqicReU3on1tnC79CZKoU130_assertion
{
miriam-gene:3133
a
ncit:C16612
.
lld:C0494261
a
ncit:C7057
.
dgn-gda:DGNca7627bb3a80e4efd6a4132fa210e26b
sio:SIO_000628
miriam-gene:3133
,
lld:C0494261
;
a
sio:SIO_001121
.
}
dgn-np:NP336579.RAJ7z9Z-Zon-9e0UlL2so7oppqicReU3on1tnC79CZKoU130_provenance
{
dgn-np:NP336579.RAJ7z9Z-Zon-9e0UlL2so7oppqicReU3on1tnC79CZKoU130_assertion
dcterms:description
"[Major histocompatibility complex (MHC) class II combined immunodeficiency (CID), also known as type II bare lymphocyte syndrome, is an autosomal recessive genetic disorder characterized by the complete lack of expression of MHC class II antigens.]. 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:8642248
;
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:NP336579.RAJ7z9Z-Zon-9e0UlL2so7oppqicReU3on1tnC79CZKoU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:18+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" .
}