@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP204090.RAuJZiautPG2fg8U1-ztBHegr2vSmBQAkTMOyI9XOv9qE
> .
@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:NP204090.RAuJZiautPG2fg8U1-ztBHegr2vSmBQAkTMOyI9XOv9qE130_head
{
this:
np:hasAssertion
dgn-np:NP204090.RAuJZiautPG2fg8U1-ztBHegr2vSmBQAkTMOyI9XOv9qE130_assertion
;
np:hasProvenance
dgn-np:NP204090.RAuJZiautPG2fg8U1-ztBHegr2vSmBQAkTMOyI9XOv9qE130_provenance
;
np:hasPublicationInfo
dgn-np:NP204090.RAuJZiautPG2fg8U1-ztBHegr2vSmBQAkTMOyI9XOv9qE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP204090.RAuJZiautPG2fg8U1-ztBHegr2vSmBQAkTMOyI9XOv9qE130_assertion
a
np:Assertion
.
dgn-np:NP204090.RAuJZiautPG2fg8U1-ztBHegr2vSmBQAkTMOyI9XOv9qE130_provenance
a
np:Provenance
.
dgn-np:NP204090.RAuJZiautPG2fg8U1-ztBHegr2vSmBQAkTMOyI9XOv9qE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP204090.RAuJZiautPG2fg8U1-ztBHegr2vSmBQAkTMOyI9XOv9qE130_assertion
{
miriam-gene:941
a
ncit:C16612
.
lld:C0027726
a
ncit:C7057
.
dgn-gda:DGNe5fc70cb5b8fcc891a3e6e9ab0be865a
sio:SIO_000628
miriam-gene:941
,
lld:C0027726
;
a
sio:SIO_001121
.
}
dgn-np:NP204090.RAuJZiautPG2fg8U1-ztBHegr2vSmBQAkTMOyI9XOv9qE130_provenance
{
dgn-np:NP204090.RAuJZiautPG2fg8U1-ztBHegr2vSmBQAkTMOyI9XOv9qE130_assertion
dcterms:description
"[Minimal change disease (MCD) is the most common cause of nephrotic syndrome in children and is associated with the expression of CD80 in podocytes and the increased excretion of CD80 in urine.]. 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:23689904
;
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:NP204090.RAuJZiautPG2fg8U1-ztBHegr2vSmBQAkTMOyI9XOv9qE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:52+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" .
}