@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP251588.RAqZ5WRzlzBrr-T6Z266nZ2WdN7y-NwYY4y38Fmt92lFc
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP251588.RAqZ5WRzlzBrr-T6Z266nZ2WdN7y-NwYY4y38Fmt92lFc130_head
{
this:
np:hasAssertion
dgn-np:NP251588.RAqZ5WRzlzBrr-T6Z266nZ2WdN7y-NwYY4y38Fmt92lFc130_assertion
;
np:hasProvenance
dgn-np:NP251588.RAqZ5WRzlzBrr-T6Z266nZ2WdN7y-NwYY4y38Fmt92lFc130_provenance
;
np:hasPublicationInfo
dgn-np:NP251588.RAqZ5WRzlzBrr-T6Z266nZ2WdN7y-NwYY4y38Fmt92lFc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP251588.RAqZ5WRzlzBrr-T6Z266nZ2WdN7y-NwYY4y38Fmt92lFc130_assertion
a
np:Assertion
.
dgn-np:NP251588.RAqZ5WRzlzBrr-T6Z266nZ2WdN7y-NwYY4y38Fmt92lFc130_provenance
a
np:Provenance
.
dgn-np:NP251588.RAqZ5WRzlzBrr-T6Z266nZ2WdN7y-NwYY4y38Fmt92lFc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP251588.RAqZ5WRzlzBrr-T6Z266nZ2WdN7y-NwYY4y38Fmt92lFc130_assertion
{
miriam-gene:5897
a
ncit:C16612
.
lld:C1801959
a
ncit:C7057
.
dgn-gda:DGN612e68dd0f6950de2b02a9b603f2244e
sio:SIO_000628
miriam-gene:5897
,
lld:C1801959
;
a
sio:SIO_001121
.
}
dgn-np:NP251588.RAqZ5WRzlzBrr-T6Z266nZ2WdN7y-NwYY4y38Fmt92lFc130_provenance
{
dgn-np:NP251588.RAqZ5WRzlzBrr-T6Z266nZ2WdN7y-NwYY4y38Fmt92lFc130_assertion
dcterms:description
"[We have recently shown that mutations that impair, but do not completely abolish the function of Rag1 and Rag2 in humans result in Omenn syndrome, an enigmatic form of combined immune deficiency characterized by oligoclonal, activated T lymphocytes with a skewed Th2 profile.]. 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:10226883
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP251588.RAqZ5WRzlzBrr-T6Z266nZ2WdN7y-NwYY4y38Fmt92lFc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:40+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}