@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP291142.RAYxbUbNI9tdbdKsInBi5rv9kGPigv86RbAiRVBlDSITs
> .
@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:NP291142.RAYxbUbNI9tdbdKsInBi5rv9kGPigv86RbAiRVBlDSITs130_head
{
this:
np:hasAssertion
dgn-np:NP291142.RAYxbUbNI9tdbdKsInBi5rv9kGPigv86RbAiRVBlDSITs130_assertion
;
np:hasProvenance
dgn-np:NP291142.RAYxbUbNI9tdbdKsInBi5rv9kGPigv86RbAiRVBlDSITs130_provenance
;
np:hasPublicationInfo
dgn-np:NP291142.RAYxbUbNI9tdbdKsInBi5rv9kGPigv86RbAiRVBlDSITs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP291142.RAYxbUbNI9tdbdKsInBi5rv9kGPigv86RbAiRVBlDSITs130_assertion
a
np:Assertion
.
dgn-np:NP291142.RAYxbUbNI9tdbdKsInBi5rv9kGPigv86RbAiRVBlDSITs130_provenance
a
np:Provenance
.
dgn-np:NP291142.RAYxbUbNI9tdbdKsInBi5rv9kGPigv86RbAiRVBlDSITs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP291142.RAYxbUbNI9tdbdKsInBi5rv9kGPigv86RbAiRVBlDSITs130_assertion
{
miriam-gene:7490
a
ncit:C16612
.
lld:C0403397
a
ncit:C7057
.
dgn-gda:DGNb66451bcbf292f5bcfcdfc88bce276e0
sio:SIO_000628
miriam-gene:7490
,
lld:C0403397
;
a
sio:SIO_001121
.
}
dgn-np:NP291142.RAYxbUbNI9tdbdKsInBi5rv9kGPigv86RbAiRVBlDSITs130_provenance
{
dgn-np:NP291142.RAYxbUbNI9tdbdKsInBi5rv9kGPigv86RbAiRVBlDSITs130_assertion
dcterms:description
"[This study further illustrates that investigation of WT1 gene mutations is clinically useful to support definitive diagnosis in children presenting with SRNS in order to direct the most appropriate clinical management.]. 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:21499692
;
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:NP291142.RAYxbUbNI9tdbdKsInBi5rv9kGPigv86RbAiRVBlDSITs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:45+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" .
}