@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP449892.RA5NP02Bu4fPlEw5anh6cTDIjOYQq08LZsBccnRzI3Spc
> .
@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:NP449892.RA5NP02Bu4fPlEw5anh6cTDIjOYQq08LZsBccnRzI3Spc130_head
{
this:
np:hasAssertion
dgn-np:NP449892.RA5NP02Bu4fPlEw5anh6cTDIjOYQq08LZsBccnRzI3Spc130_assertion
;
np:hasProvenance
dgn-np:NP449892.RA5NP02Bu4fPlEw5anh6cTDIjOYQq08LZsBccnRzI3Spc130_provenance
;
np:hasPublicationInfo
dgn-np:NP449892.RA5NP02Bu4fPlEw5anh6cTDIjOYQq08LZsBccnRzI3Spc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP449892.RA5NP02Bu4fPlEw5anh6cTDIjOYQq08LZsBccnRzI3Spc130_assertion
a
np:Assertion
.
dgn-np:NP449892.RA5NP02Bu4fPlEw5anh6cTDIjOYQq08LZsBccnRzI3Spc130_provenance
a
np:Provenance
.
dgn-np:NP449892.RA5NP02Bu4fPlEw5anh6cTDIjOYQq08LZsBccnRzI3Spc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP449892.RA5NP02Bu4fPlEw5anh6cTDIjOYQq08LZsBccnRzI3Spc130_assertion
{
miriam-gene:259
a
ncit:C16612
.
lld:C0262380
a
ncit:C7057
.
dgn-gda:DGN4bcf228fc1259c0fff3682a8f54e54fb
sio:SIO_000628
miriam-gene:259
,
lld:C0262380
;
a
sio:SIO_001121
.
}
dgn-np:NP449892.RA5NP02Bu4fPlEw5anh6cTDIjOYQq08LZsBccnRzI3Spc130_provenance
{
dgn-np:NP449892.RA5NP02Bu4fPlEw5anh6cTDIjOYQq08LZsBccnRzI3Spc130_assertion
dcterms:description
"[By modifying specific aspects of the innate immune response to UTI, genetic variation either exaggerates the severity of acute pyelonephritis to include urosepsis and renal scarring or protects against symptomatic disease by suppressing innate immune signaling, as in asymptomatic bacteriuria (ABU).]. 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:21750501
;
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:NP449892.RA5NP02Bu4fPlEw5anh6cTDIjOYQq08LZsBccnRzI3Spc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:28+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" .
}