@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP520596.RAEuzeiTsS_PiUd9xx_CIwuLRdF99fQ_f7WgkjyzkPFpY
> .
@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:NP520596.RAEuzeiTsS_PiUd9xx_CIwuLRdF99fQ_f7WgkjyzkPFpY130_head
{
this:
np:hasAssertion
dgn-np:NP520596.RAEuzeiTsS_PiUd9xx_CIwuLRdF99fQ_f7WgkjyzkPFpY130_assertion
;
np:hasProvenance
dgn-np:NP520596.RAEuzeiTsS_PiUd9xx_CIwuLRdF99fQ_f7WgkjyzkPFpY130_provenance
;
np:hasPublicationInfo
dgn-np:NP520596.RAEuzeiTsS_PiUd9xx_CIwuLRdF99fQ_f7WgkjyzkPFpY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP520596.RAEuzeiTsS_PiUd9xx_CIwuLRdF99fQ_f7WgkjyzkPFpY130_assertion
a
np:Assertion
.
dgn-np:NP520596.RAEuzeiTsS_PiUd9xx_CIwuLRdF99fQ_f7WgkjyzkPFpY130_provenance
a
np:Provenance
.
dgn-np:NP520596.RAEuzeiTsS_PiUd9xx_CIwuLRdF99fQ_f7WgkjyzkPFpY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP520596.RAEuzeiTsS_PiUd9xx_CIwuLRdF99fQ_f7WgkjyzkPFpY130_assertion
{
miriam-gene:9051
a
ncit:C16612
.
lld:C1692886
a
ncit:C7057
.
dgn-gda:DGNf31ae4d3d37cdd9bdf34d215d523188a
sio:SIO_000628
miriam-gene:9051
,
lld:C1692886
;
a
sio:SIO_001121
.
}
dgn-np:NP520596.RAEuzeiTsS_PiUd9xx_CIwuLRdF99fQ_f7WgkjyzkPFpY130_provenance
{
dgn-np:NP520596.RAEuzeiTsS_PiUd9xx_CIwuLRdF99fQ_f7WgkjyzkPFpY130_assertion
dcterms:description
"[Although common features of human PAPA syndrome such as pyogenic arthritis and skin inflammation were not recapitulated in the mouse model, ectopic expression of the mutant but not the wild type PSTPIP1 in mice lead to partial embryonic lethality, growth retardation, and elevated level of circulating proinflammatory cytokines.]. 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:23293022
;
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:NP520596.RAEuzeiTsS_PiUd9xx_CIwuLRdF99fQ_f7WgkjyzkPFpY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:10+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" .
}