@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP586137.RAL_6N8vbrJacCt4FRafSbG5AXNAr0kT9Hy9iuzGMRScM
> .
@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:NP586137.RAL_6N8vbrJacCt4FRafSbG5AXNAr0kT9Hy9iuzGMRScM130_head
{
this:
np:hasAssertion
dgn-np:NP586137.RAL_6N8vbrJacCt4FRafSbG5AXNAr0kT9Hy9iuzGMRScM130_assertion
;
np:hasProvenance
dgn-np:NP586137.RAL_6N8vbrJacCt4FRafSbG5AXNAr0kT9Hy9iuzGMRScM130_provenance
;
np:hasPublicationInfo
dgn-np:NP586137.RAL_6N8vbrJacCt4FRafSbG5AXNAr0kT9Hy9iuzGMRScM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP586137.RAL_6N8vbrJacCt4FRafSbG5AXNAr0kT9Hy9iuzGMRScM130_assertion
a
np:Assertion
.
dgn-np:NP586137.RAL_6N8vbrJacCt4FRafSbG5AXNAr0kT9Hy9iuzGMRScM130_provenance
a
np:Provenance
.
dgn-np:NP586137.RAL_6N8vbrJacCt4FRafSbG5AXNAr0kT9Hy9iuzGMRScM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP586137.RAL_6N8vbrJacCt4FRafSbG5AXNAr0kT9Hy9iuzGMRScM130_assertion
{
miriam-gene:841
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGN5136586a7430d442dbe03fae161b2a87
sio:SIO_000628
miriam-gene:841
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP586137.RAL_6N8vbrJacCt4FRafSbG5AXNAr0kT9Hy9iuzGMRScM130_provenance
{
dgn-np:NP586137.RAL_6N8vbrJacCt4FRafSbG5AXNAr0kT9Hy9iuzGMRScM130_assertion
dcterms:description
"[Our findings suggest that methylation commonly contributes to CASP8 silencing in medulloblastomas and that homozygous deletion or severe sequence changes involving the promoter region may be another mechanism leading to CASP8 inactivation in this neoplasm.]. 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:15289853
;
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:NP586137.RAL_6N8vbrJacCt4FRafSbG5AXNAr0kT9Hy9iuzGMRScM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:53+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" .
}