@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP960368.RASqhZaqadeKgxVJTPJ6Fn6TOPOlCzOCLL59SkvtE6la4
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP960368.RASqhZaqadeKgxVJTPJ6Fn6TOPOlCzOCLL59SkvtE6la4130_head
{
this:
np:hasAssertion
dgn-np:NP960368.RASqhZaqadeKgxVJTPJ6Fn6TOPOlCzOCLL59SkvtE6la4130_assertion
;
np:hasProvenance
dgn-np:NP960368.RASqhZaqadeKgxVJTPJ6Fn6TOPOlCzOCLL59SkvtE6la4130_provenance
;
np:hasPublicationInfo
dgn-np:NP960368.RASqhZaqadeKgxVJTPJ6Fn6TOPOlCzOCLL59SkvtE6la4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP960368.RASqhZaqadeKgxVJTPJ6Fn6TOPOlCzOCLL59SkvtE6la4130_assertion
a
np:Assertion
.
dgn-np:NP960368.RASqhZaqadeKgxVJTPJ6Fn6TOPOlCzOCLL59SkvtE6la4130_provenance
a
np:Provenance
.
dgn-np:NP960368.RASqhZaqadeKgxVJTPJ6Fn6TOPOlCzOCLL59SkvtE6la4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP960368.RASqhZaqadeKgxVJTPJ6Fn6TOPOlCzOCLL59SkvtE6la4130_assertion
{
miriam-gene:3577
a
ncit:C16612
.
lld:C0520575
a
ncit:C7057
.
dgn-gda:DGNb986e90d5cd7266e9ca647ec341be396
sio:SIO_000628
miriam-gene:3577
,
lld:C0520575
;
a
sio:SIO_001121
.
}
dgn-np:NP960368.RASqhZaqadeKgxVJTPJ6Fn6TOPOlCzOCLL59SkvtE6la4130_provenance
{
dgn-np:NP960368.RASqhZaqadeKgxVJTPJ6Fn6TOPOlCzOCLL59SkvtE6la4130_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-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP960368.RASqhZaqadeKgxVJTPJ6Fn6TOPOlCzOCLL59SkvtE6la4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:00+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}