@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP937396.RAb3q0dU7axQJ8BStJd2l69HRuzZxEg5EBeW6Ktb5acFU
> .
@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:NP937396.RAb3q0dU7axQJ8BStJd2l69HRuzZxEg5EBeW6Ktb5acFU130_head
{
this:
np:hasAssertion
dgn-np:NP937396.RAb3q0dU7axQJ8BStJd2l69HRuzZxEg5EBeW6Ktb5acFU130_assertion
;
np:hasProvenance
dgn-np:NP937396.RAb3q0dU7axQJ8BStJd2l69HRuzZxEg5EBeW6Ktb5acFU130_provenance
;
np:hasPublicationInfo
dgn-np:NP937396.RAb3q0dU7axQJ8BStJd2l69HRuzZxEg5EBeW6Ktb5acFU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP937396.RAb3q0dU7axQJ8BStJd2l69HRuzZxEg5EBeW6Ktb5acFU130_assertion
a
np:Assertion
.
dgn-np:NP937396.RAb3q0dU7axQJ8BStJd2l69HRuzZxEg5EBeW6Ktb5acFU130_provenance
a
np:Provenance
.
dgn-np:NP937396.RAb3q0dU7axQJ8BStJd2l69HRuzZxEg5EBeW6Ktb5acFU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP937396.RAb3q0dU7axQJ8BStJd2l69HRuzZxEg5EBeW6Ktb5acFU130_assertion
{
miriam-gene:7490
a
ncit:C16612
.
lld:C0178664
a
ncit:C7057
.
dgn-gda:DGNf95553ccd5a7c74a7eadc09034259fa7
sio:SIO_000628
miriam-gene:7490
,
lld:C0178664
;
a
sio:SIO_001121
.
}
dgn-np:NP937396.RAb3q0dU7axQJ8BStJd2l69HRuzZxEg5EBeW6Ktb5acFU130_provenance
{
dgn-np:NP937396.RAb3q0dU7axQJ8BStJd2l69HRuzZxEg5EBeW6Ktb5acFU130_assertion
dcterms:description
"[Familial cases of WT1 mutations are rare with only few cases described in the literature, whereas cases of WT1 mutations associated with isolated nephrotic proteinuria with or without focal segmental glomerular sclerosis (FSGS) are even rarer.]. 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:24161391
;
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:NP937396.RAb3q0dU7axQJ8BStJd2l69HRuzZxEg5EBeW6Ktb5acFU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:34+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" .
}