@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP833314.RAvLUKEmAN4ku668JAdGIC9TpMbAAbe-erMwnVyCsYfxw
> .
@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:NP833314.RAvLUKEmAN4ku668JAdGIC9TpMbAAbe-erMwnVyCsYfxw130_head
{
this:
np:hasAssertion
dgn-np:NP833314.RAvLUKEmAN4ku668JAdGIC9TpMbAAbe-erMwnVyCsYfxw130_assertion
;
np:hasProvenance
dgn-np:NP833314.RAvLUKEmAN4ku668JAdGIC9TpMbAAbe-erMwnVyCsYfxw130_provenance
;
np:hasPublicationInfo
dgn-np:NP833314.RAvLUKEmAN4ku668JAdGIC9TpMbAAbe-erMwnVyCsYfxw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP833314.RAvLUKEmAN4ku668JAdGIC9TpMbAAbe-erMwnVyCsYfxw130_assertion
a
np:Assertion
.
dgn-np:NP833314.RAvLUKEmAN4ku668JAdGIC9TpMbAAbe-erMwnVyCsYfxw130_provenance
a
np:Provenance
.
dgn-np:NP833314.RAvLUKEmAN4ku668JAdGIC9TpMbAAbe-erMwnVyCsYfxw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP833314.RAvLUKEmAN4ku668JAdGIC9TpMbAAbe-erMwnVyCsYfxw130_assertion
{
miriam-gene:7490
a
ncit:C16612
.
lld:C0040558
a
ncit:C7057
.
dgn-gda:DGN1c6f2d4dac2544d35005c384862cf9af
sio:SIO_000628
miriam-gene:7490
,
lld:C0040558
;
a
sio:SIO_001121
.
}
dgn-np:NP833314.RAvLUKEmAN4ku668JAdGIC9TpMbAAbe-erMwnVyCsYfxw130_provenance
{
dgn-np:NP833314.RAvLUKEmAN4ku668JAdGIC9TpMbAAbe-erMwnVyCsYfxw130_assertion
dcterms:description
"[Nephrotic syndrome (NS) in infancy includes NS of Finnish type (mutation of the nephrin gene), diffuse mesangial sclerosis (idiopathic or linked to WT1 mutation), idiopathic NS, most often steroid resistant, and NS related to infections during pregnancy (virus, syphilis, toxoplasmosis).]. 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:15682315
;
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:NP833314.RAvLUKEmAN4ku668JAdGIC9TpMbAAbe-erMwnVyCsYfxw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:30+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" .
}