@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP979622.RAz8HLBAtg5boVVdt4Iw4Pf94uzZ07DaMCG0gwbKR7Vgw
> .
@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/v3.0.0/void/
> .
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{
this:
np:hasAssertion
dgn-np:NP979622.RAz8HLBAtg5boVVdt4Iw4Pf94uzZ07DaMCG0gwbKR7Vgw130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP979622.RAz8HLBAtg5boVVdt4Iw4Pf94uzZ07DaMCG0gwbKR7Vgw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP979622.RAz8HLBAtg5boVVdt4Iw4Pf94uzZ07DaMCG0gwbKR7Vgw130_assertion
a
np:Assertion
.
dgn-np:NP979622.RAz8HLBAtg5boVVdt4Iw4Pf94uzZ07DaMCG0gwbKR7Vgw130_provenance
a
np:Provenance
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dgn-np:NP979622.RAz8HLBAtg5boVVdt4Iw4Pf94uzZ07DaMCG0gwbKR7Vgw130_publicationInfo
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.
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{
miriam-gene:201294
a
ncit:C16612
.
lld:C3495559
a
ncit:C7057
.
dgn-gda:DGN85ab522ffed4158498de9b66a62d7093
sio:SIO_000628
miriam-gene:201294
,
lld:C3495559
;
a
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.
}
dgn-np:NP979622.RAz8HLBAtg5boVVdt4Iw4Pf94uzZ07DaMCG0gwbKR7Vgw130_provenance
{
dgn-np:NP979622.RAz8HLBAtg5boVVdt4Iw4Pf94uzZ07DaMCG0gwbKR7Vgw130_assertion
dcterms:description
"[To investigate whether single-nucleotide polymorphisms (SNPs) within the genes PRF1, GZMB, UNC13D, and Rab27a, which are involved in natural killer cell dysfunction and known to contribute to the risk of hemophagocytic lymphohistiocytosis (HLH), confer an increased risk of susceptibility to systemic-onset juvenile idiopathic arthritis (JIA).]. 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:18311812
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP979622.RAz8HLBAtg5boVVdt4Iw4Pf94uzZ07DaMCG0gwbKR7Vgw130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:38+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
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;
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
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"v3.0.0" .
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