@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP679954.RA8kE1i9MkUchq-YTXXMHmWjkiu41JGt7Ufw6z0FNtE-w
> .
@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:NP679954.RA8kE1i9MkUchq-YTXXMHmWjkiu41JGt7Ufw6z0FNtE-w130_head
{
this:
np:hasAssertion
dgn-np:NP679954.RA8kE1i9MkUchq-YTXXMHmWjkiu41JGt7Ufw6z0FNtE-w130_assertion
;
np:hasProvenance
dgn-np:NP679954.RA8kE1i9MkUchq-YTXXMHmWjkiu41JGt7Ufw6z0FNtE-w130_provenance
;
np:hasPublicationInfo
dgn-np:NP679954.RA8kE1i9MkUchq-YTXXMHmWjkiu41JGt7Ufw6z0FNtE-w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP679954.RA8kE1i9MkUchq-YTXXMHmWjkiu41JGt7Ufw6z0FNtE-w130_assertion
a
np:Assertion
.
dgn-np:NP679954.RA8kE1i9MkUchq-YTXXMHmWjkiu41JGt7Ufw6z0FNtE-w130_provenance
a
np:Provenance
.
dgn-np:NP679954.RA8kE1i9MkUchq-YTXXMHmWjkiu41JGt7Ufw6z0FNtE-w130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:3718
a
ncit:C16612
.
lld:C0259743
a
ncit:C7057
.
dgn-gda:DGN0ebfcf24bd88514b31d495a554260a83
sio:SIO_000628
miriam-gene:3718
,
lld:C0259743
;
a
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.
}
dgn-np:NP679954.RA8kE1i9MkUchq-YTXXMHmWjkiu41JGt7Ufw6z0FNtE-w130_provenance
{
dgn-np:NP679954.RA8kE1i9MkUchq-YTXXMHmWjkiu41JGt7Ufw6z0FNtE-w130_assertion
dcterms:description
"[We discuss how the identification of mutations of Jak3 in autosomal recessive SCID has facilitated the diagnosis of these disorders, offered new insights into the biology of this kinase, permitted new avenues for therapy, and provided the rationale for a generation of a new class of immunosuppressants.]. 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:15661026
;
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:NP679954.RA8kE1i9MkUchq-YTXXMHmWjkiu41JGt7Ufw6z0FNtE-w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:50+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" .
}