@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP879713.RAMYMMjBv6-68UrP779jgSdmILY06j4wAbMwKHAU6B0gQ
> .
@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:NP879713.RAMYMMjBv6-68UrP779jgSdmILY06j4wAbMwKHAU6B0gQ130_head
{
this:
np:hasAssertion
dgn-np:NP879713.RAMYMMjBv6-68UrP779jgSdmILY06j4wAbMwKHAU6B0gQ130_assertion
;
np:hasProvenance
dgn-np:NP879713.RAMYMMjBv6-68UrP779jgSdmILY06j4wAbMwKHAU6B0gQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP879713.RAMYMMjBv6-68UrP779jgSdmILY06j4wAbMwKHAU6B0gQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP879713.RAMYMMjBv6-68UrP779jgSdmILY06j4wAbMwKHAU6B0gQ130_assertion
a
np:Assertion
.
dgn-np:NP879713.RAMYMMjBv6-68UrP779jgSdmILY06j4wAbMwKHAU6B0gQ130_provenance
a
np:Provenance
.
dgn-np:NP879713.RAMYMMjBv6-68UrP779jgSdmILY06j4wAbMwKHAU6B0gQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP879713.RAMYMMjBv6-68UrP779jgSdmILY06j4wAbMwKHAU6B0gQ130_assertion
{
miriam-gene:2804
a
ncit:C16612
.
lld:C0595905
a
ncit:C7057
.
dgn-gda:DGNc26fe7fdc0b2cb6ee70e45be70b8a604
sio:SIO_000628
miriam-gene:2804
,
lld:C0595905
;
a
sio:SIO_001121
.
}
dgn-np:NP879713.RAMYMMjBv6-68UrP779jgSdmILY06j4wAbMwKHAU6B0gQ130_provenance
{
dgn-np:NP879713.RAMYMMjBv6-68UrP779jgSdmILY06j4wAbMwKHAU6B0gQ130_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:NP879713.RAMYMMjBv6-68UrP779jgSdmILY06j4wAbMwKHAU6B0gQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:57+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" .
}