@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP553073.RAMS4kthyYKYrn5GDPecvHAd_Mv7b_Fyg5dcxbjF387ic
> .
@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:NP553073.RAMS4kthyYKYrn5GDPecvHAd_Mv7b_Fyg5dcxbjF387ic130_head
{
this:
np:hasAssertion
dgn-np:NP553073.RAMS4kthyYKYrn5GDPecvHAd_Mv7b_Fyg5dcxbjF387ic130_assertion
;
np:hasProvenance
dgn-np:NP553073.RAMS4kthyYKYrn5GDPecvHAd_Mv7b_Fyg5dcxbjF387ic130_provenance
;
np:hasPublicationInfo
dgn-np:NP553073.RAMS4kthyYKYrn5GDPecvHAd_Mv7b_Fyg5dcxbjF387ic130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP553073.RAMS4kthyYKYrn5GDPecvHAd_Mv7b_Fyg5dcxbjF387ic130_assertion
a
np:Assertion
.
dgn-np:NP553073.RAMS4kthyYKYrn5GDPecvHAd_Mv7b_Fyg5dcxbjF387ic130_provenance
a
np:Provenance
.
dgn-np:NP553073.RAMS4kthyYKYrn5GDPecvHAd_Mv7b_Fyg5dcxbjF387ic130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP553073.RAMS4kthyYKYrn5GDPecvHAd_Mv7b_Fyg5dcxbjF387ic130_assertion
{
miriam-gene:7827
a
ncit:C16612
.
lld:C0403397
a
ncit:C7057
.
dgn-gda:DGNec4afebbdf11e38cf6673c9a96b9d92c
sio:SIO_000628
miriam-gene:7827
,
lld:C0403397
;
a
sio:SIO_001121
.
}
dgn-np:NP553073.RAMS4kthyYKYrn5GDPecvHAd_Mv7b_Fyg5dcxbjF387ic130_provenance
{
dgn-np:NP553073.RAMS4kthyYKYrn5GDPecvHAd_Mv7b_Fyg5dcxbjF387ic130_assertion
dcterms:description
"[It was concluded that patients with steroid resistant nephrotic syndrome (SRNS) with homozygous or compound heterozygous mutations in NPHS2 have reduced risk for recurrence of focal segmental glomerulosclerosis (FSGS) in renal transplant (only 8% in comparison with 35% in patients without mutation in NPHS2).]. 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:16752799
;
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:NP553073.RAMS4kthyYKYrn5GDPecvHAd_Mv7b_Fyg5dcxbjF387ic130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:55+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" .
}