@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP266247.RAh4QmUISTZiZkIG60TaOMnI-mfY2BuAQ46C4MCe62IDk
> .
@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:NP266247.RAh4QmUISTZiZkIG60TaOMnI-mfY2BuAQ46C4MCe62IDk130_head
{
this:
np:hasAssertion
dgn-np:NP266247.RAh4QmUISTZiZkIG60TaOMnI-mfY2BuAQ46C4MCe62IDk130_assertion
;
np:hasProvenance
dgn-np:NP266247.RAh4QmUISTZiZkIG60TaOMnI-mfY2BuAQ46C4MCe62IDk130_provenance
;
np:hasPublicationInfo
dgn-np:NP266247.RAh4QmUISTZiZkIG60TaOMnI-mfY2BuAQ46C4MCe62IDk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP266247.RAh4QmUISTZiZkIG60TaOMnI-mfY2BuAQ46C4MCe62IDk130_assertion
a
np:Assertion
.
dgn-np:NP266247.RAh4QmUISTZiZkIG60TaOMnI-mfY2BuAQ46C4MCe62IDk130_provenance
a
np:Provenance
.
dgn-np:NP266247.RAh4QmUISTZiZkIG60TaOMnI-mfY2BuAQ46C4MCe62IDk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP266247.RAh4QmUISTZiZkIG60TaOMnI-mfY2BuAQ46C4MCe62IDk130_assertion
{
miriam-gene:7099
a
ncit:C16612
.
lld:C0262380
a
ncit:C7057
.
dgn-gda:DGN6bc2831f1bde076c982520f731550e20
sio:SIO_000628
miriam-gene:7099
,
lld:C0262380
;
a
sio:SIO_001121
.
}
dgn-np:NP266247.RAh4QmUISTZiZkIG60TaOMnI-mfY2BuAQ46C4MCe62IDk130_provenance
{
dgn-np:NP266247.RAh4QmUISTZiZkIG60TaOMnI-mfY2BuAQ46C4MCe62IDk130_assertion
dcterms:description
"[For example, genetic alterations that reduce TLR4 function are associated with ABU, while polymorphisms reducing IRF3 or CXCR1 expression are associated with acute pyelonephritis and an increased risk for renal scarring.]. 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:22327887
;
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:NP266247.RAh4QmUISTZiZkIG60TaOMnI-mfY2BuAQ46C4MCe62IDk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:28+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" .
}