@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP31699.RAhezvV4cuRQYo2zyBeZ77KChotrrU7cL6TPfZdFZi-aA
> .
@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:NP31699.RAhezvV4cuRQYo2zyBeZ77KChotrrU7cL6TPfZdFZi-aA130_head
{
this:
np:hasAssertion
dgn-np:NP31699.RAhezvV4cuRQYo2zyBeZ77KChotrrU7cL6TPfZdFZi-aA130_assertion
;
np:hasProvenance
dgn-np:NP31699.RAhezvV4cuRQYo2zyBeZ77KChotrrU7cL6TPfZdFZi-aA130_provenance
;
np:hasPublicationInfo
dgn-np:NP31699.RAhezvV4cuRQYo2zyBeZ77KChotrrU7cL6TPfZdFZi-aA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP31699.RAhezvV4cuRQYo2zyBeZ77KChotrrU7cL6TPfZdFZi-aA130_assertion
a
np:Assertion
.
dgn-np:NP31699.RAhezvV4cuRQYo2zyBeZ77KChotrrU7cL6TPfZdFZi-aA130_provenance
a
np:Provenance
.
dgn-np:NP31699.RAhezvV4cuRQYo2zyBeZ77KChotrrU7cL6TPfZdFZi-aA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP31699.RAhezvV4cuRQYo2zyBeZ77KChotrrU7cL6TPfZdFZi-aA130_assertion
{
miriam-gene:7040
a
ncit:C16612
.
lld:C0027726
a
ncit:C7057
.
dgn-gda:DGNeaf274533017963149593ff0a079b100
sio:SIO_000628
miriam-gene:7040
,
lld:C0027726
;
a
sio:SIO_001121
.
}
dgn-np:NP31699.RAhezvV4cuRQYo2zyBeZ77KChotrrU7cL6TPfZdFZi-aA130_provenance
{
dgn-np:NP31699.RAhezvV4cuRQYo2zyBeZ77KChotrrU7cL6TPfZdFZi-aA130_assertion
dcterms:description
"[Nephrotic syndrome induced by puromycin aminonucleoside (PAN) is characterized by tubulointerstitial (TI) inflammation, foci of TI fibrosis, and increased renal mRNA levels for matrix genes, the tissue inhibitor of metalloproteinases (TIMP), and the transforming growth factor-beta 1 (TGF-beta 1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:8023968
;
prov:wasDerivedFrom
dgn-void:ctd_human-20130708
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20130708
pav:importedOn
"2013-07-24"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP31699.RAhezvV4cuRQYo2zyBeZ77KChotrrU7cL6TPfZdFZi-aA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:13+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" .
}