@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP690317.RAV72Sw0toNUale9D2F3_pDGjGB152lxfCJ3CLKqYk5y0
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP690317.RAV72Sw0toNUale9D2F3_pDGjGB152lxfCJ3CLKqYk5y0130_assertion
;
np:hasProvenance
dgn-np:NP690317.RAV72Sw0toNUale9D2F3_pDGjGB152lxfCJ3CLKqYk5y0130_provenance
;
np:hasPublicationInfo
dgn-np:NP690317.RAV72Sw0toNUale9D2F3_pDGjGB152lxfCJ3CLKqYk5y0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP690317.RAV72Sw0toNUale9D2F3_pDGjGB152lxfCJ3CLKqYk5y0130_assertion
a
np:Assertion
.
dgn-np:NP690317.RAV72Sw0toNUale9D2F3_pDGjGB152lxfCJ3CLKqYk5y0130_provenance
a
np:Provenance
.
dgn-np:NP690317.RAV72Sw0toNUale9D2F3_pDGjGB152lxfCJ3CLKqYk5y0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP690317.RAV72Sw0toNUale9D2F3_pDGjGB152lxfCJ3CLKqYk5y0130_assertion
{
miriam-gene:2652
a
ncit:C16612
.
lld:C0001614
a
ncit:C7057
.
dgn-gda:DGNa0246714e7ffdc031a2902c80b048ff7
sio:SIO_000628
miriam-gene:2652
,
lld:C0001614
;
a
sio:SIO_001121
.
}
dgn-np:NP690317.RAV72Sw0toNUale9D2F3_pDGjGB152lxfCJ3CLKqYk5y0130_provenance
{
dgn-np:NP690317.RAV72Sw0toNUale9D2F3_pDGjGB152lxfCJ3CLKqYk5y0130_assertion
dcterms:description
"[Medulloblastoma (MB) is the most common malignant pediatric brain tumor and is thought to arise from genetic anomalies in developmental pathways required for the normal maturation of the cerebellar cortex, notably developmental pathways for granule cell progenitor (GCP) neurogenesis.]. 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:21315459
;
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:NP690317.RAV72Sw0toNUale9D2F3_pDGjGB152lxfCJ3CLKqYk5y0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:59+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" .
}