@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP132950.RAm68UDk6491XGAsL0BZmeUkwFt1dzhV0HnrKT_Oi4RWc
> .
@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:NP132950.RAm68UDk6491XGAsL0BZmeUkwFt1dzhV0HnrKT_Oi4RWc130_head
{
this:
np:hasAssertion
dgn-np:NP132950.RAm68UDk6491XGAsL0BZmeUkwFt1dzhV0HnrKT_Oi4RWc130_assertion
;
np:hasProvenance
dgn-np:NP132950.RAm68UDk6491XGAsL0BZmeUkwFt1dzhV0HnrKT_Oi4RWc130_provenance
;
np:hasPublicationInfo
dgn-np:NP132950.RAm68UDk6491XGAsL0BZmeUkwFt1dzhV0HnrKT_Oi4RWc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP132950.RAm68UDk6491XGAsL0BZmeUkwFt1dzhV0HnrKT_Oi4RWc130_assertion
a
np:Assertion
.
dgn-np:NP132950.RAm68UDk6491XGAsL0BZmeUkwFt1dzhV0HnrKT_Oi4RWc130_provenance
a
np:Provenance
.
dgn-np:NP132950.RAm68UDk6491XGAsL0BZmeUkwFt1dzhV0HnrKT_Oi4RWc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP132950.RAm68UDk6491XGAsL0BZmeUkwFt1dzhV0HnrKT_Oi4RWc130_assertion
{
miriam-gene:7490
a
ncit:C16612
.
lld:C0027726
a
ncit:C7057
.
dgn-gda:DGN4df70d769e7f61c87b454bae16d35d18
sio:SIO_000628
miriam-gene:7490
,
lld:C0027726
;
a
sio:SIO_001122
.
}
dgn-np:NP132950.RAm68UDk6491XGAsL0BZmeUkwFt1dzhV0HnrKT_Oi4RWc130_provenance
{
dgn-np:NP132950.RAm68UDk6491XGAsL0BZmeUkwFt1dzhV0HnrKT_Oi4RWc130_assertion
dcterms:description
"[mutations in the WT1 have been found to be present in patients with SRNS in association with Wilms'tumor (WT) and urinary or genital malformations, as well as in patients with isolated steroid resistant nephrotic syndrome ]. 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:15253707
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP132950.RAm68UDk6491XGAsL0BZmeUkwFt1dzhV0HnrKT_Oi4RWc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:09+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" .
}