@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP754541.RA9QaX2zZrDWYh--nWKabjSEliK6dp2TNIjA2Nqz0_oQc
> .
@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:NP754541.RA9QaX2zZrDWYh--nWKabjSEliK6dp2TNIjA2Nqz0_oQc130_head
{
this:
np:hasAssertion
dgn-np:NP754541.RA9QaX2zZrDWYh--nWKabjSEliK6dp2TNIjA2Nqz0_oQc130_assertion
;
np:hasProvenance
dgn-np:NP754541.RA9QaX2zZrDWYh--nWKabjSEliK6dp2TNIjA2Nqz0_oQc130_provenance
;
np:hasPublicationInfo
dgn-np:NP754541.RA9QaX2zZrDWYh--nWKabjSEliK6dp2TNIjA2Nqz0_oQc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP754541.RA9QaX2zZrDWYh--nWKabjSEliK6dp2TNIjA2Nqz0_oQc130_assertion
a
np:Assertion
.
dgn-np:NP754541.RA9QaX2zZrDWYh--nWKabjSEliK6dp2TNIjA2Nqz0_oQc130_provenance
a
np:Provenance
.
dgn-np:NP754541.RA9QaX2zZrDWYh--nWKabjSEliK6dp2TNIjA2Nqz0_oQc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP754541.RA9QaX2zZrDWYh--nWKabjSEliK6dp2TNIjA2Nqz0_oQc130_assertion
{
miriam-gene:4210
a
ncit:C16612
.
lld:C0243026
a
ncit:C7057
.
dgn-gda:DGNa81086b2955eff875c145711a6f204f2
sio:SIO_000628
miriam-gene:4210
,
lld:C0243026
;
a
sio:SIO_001121
.
}
dgn-np:NP754541.RA9QaX2zZrDWYh--nWKabjSEliK6dp2TNIjA2Nqz0_oQc130_provenance
{
dgn-np:NP754541.RA9QaX2zZrDWYh--nWKabjSEliK6dp2TNIjA2Nqz0_oQc130_assertion
dcterms:description
"[Our results showed that critically ill patients with SIRS and sepsis have increased prevalence of pyrin mutations, and patients with SIRS and sepsis carrying the pyrin mutation seem to be highly susceptible for a severe disease course.]. 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:17696266
;
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:NP754541.RA9QaX2zZrDWYh--nWKabjSEliK6dp2TNIjA2Nqz0_oQc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:37+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" .
}