@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP709696.RA0Uazbe1aPhsSYQJSQL0HcvV9NnSkDma-tOB9zfL9LtI
> .
@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:NP709696.RA0Uazbe1aPhsSYQJSQL0HcvV9NnSkDma-tOB9zfL9LtI130_head
{
this:
np:hasAssertion
dgn-np:NP709696.RA0Uazbe1aPhsSYQJSQL0HcvV9NnSkDma-tOB9zfL9LtI130_assertion
;
np:hasProvenance
dgn-np:NP709696.RA0Uazbe1aPhsSYQJSQL0HcvV9NnSkDma-tOB9zfL9LtI130_provenance
;
np:hasPublicationInfo
dgn-np:NP709696.RA0Uazbe1aPhsSYQJSQL0HcvV9NnSkDma-tOB9zfL9LtI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP709696.RA0Uazbe1aPhsSYQJSQL0HcvV9NnSkDma-tOB9zfL9LtI130_assertion
a
np:Assertion
.
dgn-np:NP709696.RA0Uazbe1aPhsSYQJSQL0HcvV9NnSkDma-tOB9zfL9LtI130_provenance
a
np:Provenance
.
dgn-np:NP709696.RA0Uazbe1aPhsSYQJSQL0HcvV9NnSkDma-tOB9zfL9LtI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP709696.RA0Uazbe1aPhsSYQJSQL0HcvV9NnSkDma-tOB9zfL9LtI130_assertion
{
miriam-gene:7490
a
ncit:C16612
.
lld:C1318541
a
ncit:C7057
.
dgn-gda:DGN17f1d563f4dbb27f7a38895914813831
sio:SIO_000628
miriam-gene:7490
,
lld:C1318541
;
a
sio:SIO_001121
.
}
dgn-np:NP709696.RA0Uazbe1aPhsSYQJSQL0HcvV9NnSkDma-tOB9zfL9LtI130_provenance
{
dgn-np:NP709696.RA0Uazbe1aPhsSYQJSQL0HcvV9NnSkDma-tOB9zfL9LtI130_assertion
dcterms:description
"[The expression of the Wilms' tumor suppressor gene WT1 in granulosa and Sertoli cells prompted us to analyze this gene for mutations in 11 granulosa cell tumors, three Leydig cell tumors, and one Sertoli/Leydig cell tumor.]. 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:8504409
;
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:NP709696.RA0Uazbe1aPhsSYQJSQL0HcvV9NnSkDma-tOB9zfL9LtI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:11+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" .
}