@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1079176.RAlAGAoQ_dCGNad_gxufmAtn0uEQ1lV53pTwMpYgdNC5U
> .
@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:NP1079176.RAlAGAoQ_dCGNad_gxufmAtn0uEQ1lV53pTwMpYgdNC5U130_head
{
this:
np:hasAssertion
dgn-np:NP1079176.RAlAGAoQ_dCGNad_gxufmAtn0uEQ1lV53pTwMpYgdNC5U130_assertion
;
np:hasProvenance
dgn-np:NP1079176.RAlAGAoQ_dCGNad_gxufmAtn0uEQ1lV53pTwMpYgdNC5U130_provenance
;
np:hasPublicationInfo
dgn-np:NP1079176.RAlAGAoQ_dCGNad_gxufmAtn0uEQ1lV53pTwMpYgdNC5U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1079176.RAlAGAoQ_dCGNad_gxufmAtn0uEQ1lV53pTwMpYgdNC5U130_assertion
a
np:Assertion
.
dgn-np:NP1079176.RAlAGAoQ_dCGNad_gxufmAtn0uEQ1lV53pTwMpYgdNC5U130_provenance
a
np:Provenance
.
dgn-np:NP1079176.RAlAGAoQ_dCGNad_gxufmAtn0uEQ1lV53pTwMpYgdNC5U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1079176.RAlAGAoQ_dCGNad_gxufmAtn0uEQ1lV53pTwMpYgdNC5U130_assertion
{
miriam-gene:941
a
ncit:C16612
.
lld:C0027721
a
ncit:C7057
.
dgn-gda:DGN02b5e8ee6c9d0c0b468c4fb6a506293b
sio:SIO_000628
miriam-gene:941
,
lld:C0027721
;
a
sio:SIO_001121
.
}
dgn-np:NP1079176.RAlAGAoQ_dCGNad_gxufmAtn0uEQ1lV53pTwMpYgdNC5U130_provenance
{
dgn-np:NP1079176.RAlAGAoQ_dCGNad_gxufmAtn0uEQ1lV53pTwMpYgdNC5U130_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-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:NP1079176.RAlAGAoQ_dCGNad_gxufmAtn0uEQ1lV53pTwMpYgdNC5U130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:55+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" .
}