@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP535607.RACQXEAlI6vuHf5eTGmr5_6vysIZE3_47ywg5335EYmO8
> .
@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:NP535607.RACQXEAlI6vuHf5eTGmr5_6vysIZE3_47ywg5335EYmO8130_head
{
this:
np:hasAssertion
dgn-np:NP535607.RACQXEAlI6vuHf5eTGmr5_6vysIZE3_47ywg5335EYmO8130_assertion
;
np:hasProvenance
dgn-np:NP535607.RACQXEAlI6vuHf5eTGmr5_6vysIZE3_47ywg5335EYmO8130_provenance
;
np:hasPublicationInfo
dgn-np:NP535607.RACQXEAlI6vuHf5eTGmr5_6vysIZE3_47ywg5335EYmO8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP535607.RACQXEAlI6vuHf5eTGmr5_6vysIZE3_47ywg5335EYmO8130_assertion
a
np:Assertion
.
dgn-np:NP535607.RACQXEAlI6vuHf5eTGmr5_6vysIZE3_47ywg5335EYmO8130_provenance
a
np:Provenance
.
dgn-np:NP535607.RACQXEAlI6vuHf5eTGmr5_6vysIZE3_47ywg5335EYmO8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP535607.RACQXEAlI6vuHf5eTGmr5_6vysIZE3_47ywg5335EYmO8130_assertion
{
miriam-gene:4868
a
ncit:C16612
.
lld:C0027708
a
ncit:C7057
.
dgn-gda:DGNf6ab88c48cd8067878accb9adfe28920
sio:SIO_000628
miriam-gene:4868
,
lld:C0027708
;
a
sio:SIO_001121
.
}
dgn-np:NP535607.RACQXEAlI6vuHf5eTGmr5_6vysIZE3_47ywg5335EYmO8130_provenance
{
dgn-np:NP535607.RACQXEAlI6vuHf5eTGmr5_6vysIZE3_47ywg5335EYmO8130_assertion
dcterms:description
"[Subsequently, kidneys from patients with congenital nephrotic syndrome of the Finnish type (CNF), presenting with heavy proteinuria, and Wilms' tumor tissue were studied for the corresponding expression pattern for evidence of dedifferentiation/persistence of a fetal expression pattern.]. 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:9438174
;
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:NP535607.RACQXEAlI6vuHf5eTGmr5_6vysIZE3_47ywg5335EYmO8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:23+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" .
}