@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP358742.RAvmo9JApAdwzQxys2SrBuh26TTyfzFFfqpzwyyMVk1V0
> .
@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:NP358742.RAvmo9JApAdwzQxys2SrBuh26TTyfzFFfqpzwyyMVk1V0130_head
{
this:
np:hasAssertion
dgn-np:NP358742.RAvmo9JApAdwzQxys2SrBuh26TTyfzFFfqpzwyyMVk1V0130_assertion
;
np:hasProvenance
dgn-np:NP358742.RAvmo9JApAdwzQxys2SrBuh26TTyfzFFfqpzwyyMVk1V0130_provenance
;
np:hasPublicationInfo
dgn-np:NP358742.RAvmo9JApAdwzQxys2SrBuh26TTyfzFFfqpzwyyMVk1V0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP358742.RAvmo9JApAdwzQxys2SrBuh26TTyfzFFfqpzwyyMVk1V0130_assertion
a
np:Assertion
.
dgn-np:NP358742.RAvmo9JApAdwzQxys2SrBuh26TTyfzFFfqpzwyyMVk1V0130_provenance
a
np:Provenance
.
dgn-np:NP358742.RAvmo9JApAdwzQxys2SrBuh26TTyfzFFfqpzwyyMVk1V0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP358742.RAvmo9JApAdwzQxys2SrBuh26TTyfzFFfqpzwyyMVk1V0130_assertion
{
miriam-gene:7827
a
ncit:C16612
.
lld:C0017668
a
ncit:C7057
.
dgn-gda:DGN52bf4f8fc111a0673f60a84b03fe503a
sio:SIO_000628
miriam-gene:7827
,
lld:C0017668
;
a
sio:SIO_001121
.
}
dgn-np:NP358742.RAvmo9JApAdwzQxys2SrBuh26TTyfzFFfqpzwyyMVk1V0130_provenance
{
dgn-np:NP358742.RAvmo9JApAdwzQxys2SrBuh26TTyfzFFfqpzwyyMVk1V0130_assertion
dcterms:description
"[To evaluate the incidence of posttransplant recurrence of FSGS in patients with NPHS2, the authors screened for podocin mutations in 53 patients with the clinical and pathologic stigmata of FSGS who had renal failure and who had undergone renal transplantation.Results.]. 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:12776285
;
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:NP358742.RAvmo9JApAdwzQxys2SrBuh26TTyfzFFfqpzwyyMVk1V0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:30+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" .
}