@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP808300.RAWszdLYY6R6zUVVwRrap2JyyneKjl1Vp-cpKDOfkDJZ4
> .
@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:NP808300.RAWszdLYY6R6zUVVwRrap2JyyneKjl1Vp-cpKDOfkDJZ4130_head
{
this:
np:hasAssertion
dgn-np:NP808300.RAWszdLYY6R6zUVVwRrap2JyyneKjl1Vp-cpKDOfkDJZ4130_assertion
;
np:hasProvenance
dgn-np:NP808300.RAWszdLYY6R6zUVVwRrap2JyyneKjl1Vp-cpKDOfkDJZ4130_provenance
;
np:hasPublicationInfo
dgn-np:NP808300.RAWszdLYY6R6zUVVwRrap2JyyneKjl1Vp-cpKDOfkDJZ4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP808300.RAWszdLYY6R6zUVVwRrap2JyyneKjl1Vp-cpKDOfkDJZ4130_assertion
a
np:Assertion
.
dgn-np:NP808300.RAWszdLYY6R6zUVVwRrap2JyyneKjl1Vp-cpKDOfkDJZ4130_provenance
a
np:Provenance
.
dgn-np:NP808300.RAWszdLYY6R6zUVVwRrap2JyyneKjl1Vp-cpKDOfkDJZ4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP808300.RAWszdLYY6R6zUVVwRrap2JyyneKjl1Vp-cpKDOfkDJZ4130_assertion
{
miriam-gene:834
a
ncit:C16612
.
lld:C0268390
a
ncit:C7057
.
dgn-gda:DGN359ee52262a926aa9a14d18f6a01511b
sio:SIO_000628
miriam-gene:834
,
lld:C0268390
;
a
sio:SIO_001121
.
}
dgn-np:NP808300.RAWszdLYY6R6zUVVwRrap2JyyneKjl1Vp-cpKDOfkDJZ4130_provenance
{
dgn-np:NP808300.RAWszdLYY6R6zUVVwRrap2JyyneKjl1Vp-cpKDOfkDJZ4130_assertion
dcterms:description
"[The autoinflammatory disorders Muckle-Wells syndrome, familial cold urtecaria and chronic infantile neurological cutaneous and articular syndrome are associated with mutations in the NALP3 (Cryopyrin) gene, which is the central platform of the proinflammatory caspase-1 activating complex, named the inflammasome.]. 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:17431422
;
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:NP808300.RAWszdLYY6R6zUVVwRrap2JyyneKjl1Vp-cpKDOfkDJZ4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:15+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" .
}