@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP778160.RAyzMjleBAVxslsiXkB4vslOHjSOzXpsAMrOSTulLNcLg
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP778160.RAyzMjleBAVxslsiXkB4vslOHjSOzXpsAMrOSTulLNcLg130_head
{
this:
np:hasAssertion
dgn-np:NP778160.RAyzMjleBAVxslsiXkB4vslOHjSOzXpsAMrOSTulLNcLg130_assertion
;
np:hasProvenance
dgn-np:NP778160.RAyzMjleBAVxslsiXkB4vslOHjSOzXpsAMrOSTulLNcLg130_provenance
;
np:hasPublicationInfo
dgn-np:NP778160.RAyzMjleBAVxslsiXkB4vslOHjSOzXpsAMrOSTulLNcLg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP778160.RAyzMjleBAVxslsiXkB4vslOHjSOzXpsAMrOSTulLNcLg130_assertion
a
np:Assertion
.
dgn-np:NP778160.RAyzMjleBAVxslsiXkB4vslOHjSOzXpsAMrOSTulLNcLg130_provenance
a
np:Provenance
.
dgn-np:NP778160.RAyzMjleBAVxslsiXkB4vslOHjSOzXpsAMrOSTulLNcLg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP778160.RAyzMjleBAVxslsiXkB4vslOHjSOzXpsAMrOSTulLNcLg130_assertion
{
miriam-gene:7490
a
ncit:C16612
.
lld:C0022658
a
ncit:C7057
.
dgn-gda:DGN585baac375fe0b509ec4d1e5562ba4c0
sio:SIO_000628
miriam-gene:7490
,
lld:C0022658
;
a
sio:SIO_001121
.
}
dgn-np:NP778160.RAyzMjleBAVxslsiXkB4vslOHjSOzXpsAMrOSTulLNcLg130_provenance
{
dgn-np:NP778160.RAyzMjleBAVxslsiXkB4vslOHjSOzXpsAMrOSTulLNcLg130_assertion
dcterms:description
"[Although these syndromes are genetic models of nephropathy and the mutations of WT1 gene are characterized in these patients the mechanism how mutations of WT1 gene affect the embryonic kidney adversely has not been elucidated.]. 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:10586431
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP778160.RAyzMjleBAVxslsiXkB4vslOHjSOzXpsAMrOSTulLNcLg130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:30+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}