@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP309221.RA2lhHnomYTVWWeQ5JWFsWtTERYx1MKv0m4c44JavJvVg
> .
@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:NP309221.RA2lhHnomYTVWWeQ5JWFsWtTERYx1MKv0m4c44JavJvVg130_head
{
this:
np:hasAssertion
dgn-np:NP309221.RA2lhHnomYTVWWeQ5JWFsWtTERYx1MKv0m4c44JavJvVg130_assertion
;
np:hasProvenance
dgn-np:NP309221.RA2lhHnomYTVWWeQ5JWFsWtTERYx1MKv0m4c44JavJvVg130_provenance
;
np:hasPublicationInfo
dgn-np:NP309221.RA2lhHnomYTVWWeQ5JWFsWtTERYx1MKv0m4c44JavJvVg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP309221.RA2lhHnomYTVWWeQ5JWFsWtTERYx1MKv0m4c44JavJvVg130_assertion
a
np:Assertion
.
dgn-np:NP309221.RA2lhHnomYTVWWeQ5JWFsWtTERYx1MKv0m4c44JavJvVg130_provenance
a
np:Provenance
.
dgn-np:NP309221.RA2lhHnomYTVWWeQ5JWFsWtTERYx1MKv0m4c44JavJvVg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP309221.RA2lhHnomYTVWWeQ5JWFsWtTERYx1MKv0m4c44JavJvVg130_assertion
{
miriam-gene:4358
a
ncit:C16612
.
lld:C0022661
a
ncit:C7057
.
dgn-gda:DGN2c1f207743f3fe8e54e52c889bd49fd1
sio:SIO_000628
miriam-gene:4358
,
lld:C0022661
;
a
sio:SIO_001121
.
}
dgn-np:NP309221.RA2lhHnomYTVWWeQ5JWFsWtTERYx1MKv0m4c44JavJvVg130_provenance
{
dgn-np:NP309221.RA2lhHnomYTVWWeQ5JWFsWtTERYx1MKv0m4c44JavJvVg130_assertion
dcterms:description
"[A multicenter retrospective study was performed on the role of ACE genotypes and medical treatments in 43 Japanese children with FSGS (20 males and 23 females), including 17 children who progressed to end-stage renal failure during the mean observation period of 6.9 +/- (SD) 5.0 years.]. 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:11474225
;
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:NP309221.RA2lhHnomYTVWWeQ5JWFsWtTERYx1MKv0m4c44JavJvVg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:57+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" .
}