@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP546578.RABuP6jVwA205EYnNn1UciNJk3tgifsXdsg3selffvkhY
> .
@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:NP546578.RABuP6jVwA205EYnNn1UciNJk3tgifsXdsg3selffvkhY130_head
{
this:
np:hasAssertion
dgn-np:NP546578.RABuP6jVwA205EYnNn1UciNJk3tgifsXdsg3selffvkhY130_assertion
;
np:hasProvenance
dgn-np:NP546578.RABuP6jVwA205EYnNn1UciNJk3tgifsXdsg3selffvkhY130_provenance
;
np:hasPublicationInfo
dgn-np:NP546578.RABuP6jVwA205EYnNn1UciNJk3tgifsXdsg3selffvkhY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP546578.RABuP6jVwA205EYnNn1UciNJk3tgifsXdsg3selffvkhY130_assertion
a
np:Assertion
.
dgn-np:NP546578.RABuP6jVwA205EYnNn1UciNJk3tgifsXdsg3selffvkhY130_provenance
a
np:Provenance
.
dgn-np:NP546578.RABuP6jVwA205EYnNn1UciNJk3tgifsXdsg3selffvkhY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP546578.RABuP6jVwA205EYnNn1UciNJk3tgifsXdsg3selffvkhY130_assertion
{
miriam-gene:51684
a
ncit:C16612
.
lld:C0025149
a
ncit:C7057
.
dgn-gda:DGNa7b06f0063acaed61a6b99fbefa965c7
sio:SIO_000628
miriam-gene:51684
,
lld:C0025149
;
a
sio:SIO_001121
.
}
dgn-np:NP546578.RABuP6jVwA205EYnNn1UciNJk3tgifsXdsg3selffvkhY130_provenance
{
dgn-np:NP546578.RABuP6jVwA205EYnNn1UciNJk3tgifsXdsg3selffvkhY130_assertion
dcterms:description
"[A complete mutational analysis of the SUFU gene was performed on genomic DNA in all 131 consecutive patients treated for medulloblastoma in the pediatrics department of the Institut Gustave Roussy between 1972 and 2009 and for whom a blood sample was available.]. 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:22508808
;
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:NP546578.RABuP6jVwA205EYnNn1UciNJk3tgifsXdsg3selffvkhY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:29+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" .
}