@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP192508.RA122ataMjaYqEFg8ZZqSx1Hh2IU3TAMADiJwai_iV0ds
> .
@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:NP192508.RA122ataMjaYqEFg8ZZqSx1Hh2IU3TAMADiJwai_iV0ds130_head
{
this:
np:hasAssertion
dgn-np:NP192508.RA122ataMjaYqEFg8ZZqSx1Hh2IU3TAMADiJwai_iV0ds130_assertion
;
np:hasProvenance
dgn-np:NP192508.RA122ataMjaYqEFg8ZZqSx1Hh2IU3TAMADiJwai_iV0ds130_provenance
;
np:hasPublicationInfo
dgn-np:NP192508.RA122ataMjaYqEFg8ZZqSx1Hh2IU3TAMADiJwai_iV0ds130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP192508.RA122ataMjaYqEFg8ZZqSx1Hh2IU3TAMADiJwai_iV0ds130_assertion
a
np:Assertion
.
dgn-np:NP192508.RA122ataMjaYqEFg8ZZqSx1Hh2IU3TAMADiJwai_iV0ds130_provenance
a
np:Provenance
.
dgn-np:NP192508.RA122ataMjaYqEFg8ZZqSx1Hh2IU3TAMADiJwai_iV0ds130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP192508.RA122ataMjaYqEFg8ZZqSx1Hh2IU3TAMADiJwai_iV0ds130_assertion
{
miriam-gene:3133
a
ncit:C16612
.
lld:C0019247
a
ncit:C7057
.
dgn-gda:DGNe74d7d812148c32d2e386923dc382289
sio:SIO_000628
miriam-gene:3133
,
lld:C0019247
;
a
sio:SIO_001121
.
}
dgn-np:NP192508.RA122ataMjaYqEFg8ZZqSx1Hh2IU3TAMADiJwai_iV0ds130_provenance
{
dgn-np:NP192508.RA122ataMjaYqEFg8ZZqSx1Hh2IU3TAMADiJwai_iV0ds130_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:NP192508.RA122ataMjaYqEFg8ZZqSx1Hh2IU3TAMADiJwai_iV0ds130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:45+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" .
}