@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP637660.RAR4AZMdBQgLdAhEOY9k2Ubk7BRUdjejiu4KzmfFzUpso
> .
@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:NP637660.RAR4AZMdBQgLdAhEOY9k2Ubk7BRUdjejiu4KzmfFzUpso130_head
{
this:
np:hasAssertion
dgn-np:NP637660.RAR4AZMdBQgLdAhEOY9k2Ubk7BRUdjejiu4KzmfFzUpso130_assertion
;
np:hasProvenance
dgn-np:NP637660.RAR4AZMdBQgLdAhEOY9k2Ubk7BRUdjejiu4KzmfFzUpso130_provenance
;
np:hasPublicationInfo
dgn-np:NP637660.RAR4AZMdBQgLdAhEOY9k2Ubk7BRUdjejiu4KzmfFzUpso130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP637660.RAR4AZMdBQgLdAhEOY9k2Ubk7BRUdjejiu4KzmfFzUpso130_assertion
a
np:Assertion
.
dgn-np:NP637660.RAR4AZMdBQgLdAhEOY9k2Ubk7BRUdjejiu4KzmfFzUpso130_provenance
a
np:Provenance
.
dgn-np:NP637660.RAR4AZMdBQgLdAhEOY9k2Ubk7BRUdjejiu4KzmfFzUpso130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP637660.RAR4AZMdBQgLdAhEOY9k2Ubk7BRUdjejiu4KzmfFzUpso130_assertion
{
miriam-gene:7490
a
ncit:C16612
.
lld:C0042063
a
ncit:C7057
.
dgn-gda:DGN04af0dafac7bc7a3078425696408ba55
sio:SIO_000628
miriam-gene:7490
,
lld:C0042063
;
a
sio:SIO_001121
.
}
dgn-np:NP637660.RAR4AZMdBQgLdAhEOY9k2Ubk7BRUdjejiu4KzmfFzUpso130_provenance
{
dgn-np:NP637660.RAR4AZMdBQgLdAhEOY9k2Ubk7BRUdjejiu4KzmfFzUpso130_assertion
dcterms:description
"[The Wilms tumor suppressor gene, WT1, plays an important role in the development of the urogenital system and the gonads, and clinical syndromes associated with WT1 mutations, such as WAGR syndrome, Denys-Drash syndrome and Frasier syndrome, typically manifest as renal and genitourinary abnormalities.]. 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:16932893
;
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:NP637660.RAR4AZMdBQgLdAhEOY9k2Ubk7BRUdjejiu4KzmfFzUpso130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:24+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" .
}