@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP243548.RAbeQlnb1StTMRWYsNVqf9OZYNWeM6fVad5nUF0j0h-O4
> .
@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:NP243548.RAbeQlnb1StTMRWYsNVqf9OZYNWeM6fVad5nUF0j0h-O4130_head
{
this:
np:hasAssertion
dgn-np:NP243548.RAbeQlnb1StTMRWYsNVqf9OZYNWeM6fVad5nUF0j0h-O4130_assertion
;
np:hasProvenance
dgn-np:NP243548.RAbeQlnb1StTMRWYsNVqf9OZYNWeM6fVad5nUF0j0h-O4130_provenance
;
np:hasPublicationInfo
dgn-np:NP243548.RAbeQlnb1StTMRWYsNVqf9OZYNWeM6fVad5nUF0j0h-O4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP243548.RAbeQlnb1StTMRWYsNVqf9OZYNWeM6fVad5nUF0j0h-O4130_assertion
a
np:Assertion
.
dgn-np:NP243548.RAbeQlnb1StTMRWYsNVqf9OZYNWeM6fVad5nUF0j0h-O4130_provenance
a
np:Provenance
.
dgn-np:NP243548.RAbeQlnb1StTMRWYsNVqf9OZYNWeM6fVad5nUF0j0h-O4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP243548.RAbeQlnb1StTMRWYsNVqf9OZYNWeM6fVad5nUF0j0h-O4130_assertion
{
miriam-gene:7422
a
ncit:C16612
.
lld:C0268713
a
ncit:C7057
.
dgn-gda:DGN1cad211b81082ba0d67a6baa1a940969
sio:SIO_000628
miriam-gene:7422
,
lld:C0268713
;
a
sio:SIO_001121
.
}
dgn-np:NP243548.RAbeQlnb1StTMRWYsNVqf9OZYNWeM6fVad5nUF0j0h-O4130_provenance
{
dgn-np:NP243548.RAbeQlnb1StTMRWYsNVqf9OZYNWeM6fVad5nUF0j0h-O4130_assertion
dcterms:description
"[The present study was designed to clarify the proposed role of VPF in diseases with increased glomerular permeability as here exemplified by the congenital nephrotic syndrome of the Finnish type (CNF).]. 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:8910928
;
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:NP243548.RAbeQlnb1StTMRWYsNVqf9OZYNWeM6fVad5nUF0j0h-O4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:16+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" .
}