@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP462432.RAgb3OcqDeeer1SA2DP3P2ZB0nal1VQHPDzXWqT-EACFs
> .
@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:NP462432.RAgb3OcqDeeer1SA2DP3P2ZB0nal1VQHPDzXWqT-EACFs130_head
{
this:
np:hasAssertion
dgn-np:NP462432.RAgb3OcqDeeer1SA2DP3P2ZB0nal1VQHPDzXWqT-EACFs130_assertion
;
np:hasProvenance
dgn-np:NP462432.RAgb3OcqDeeer1SA2DP3P2ZB0nal1VQHPDzXWqT-EACFs130_provenance
;
np:hasPublicationInfo
dgn-np:NP462432.RAgb3OcqDeeer1SA2DP3P2ZB0nal1VQHPDzXWqT-EACFs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP462432.RAgb3OcqDeeer1SA2DP3P2ZB0nal1VQHPDzXWqT-EACFs130_assertion
a
np:Assertion
.
dgn-np:NP462432.RAgb3OcqDeeer1SA2DP3P2ZB0nal1VQHPDzXWqT-EACFs130_provenance
a
np:Provenance
.
dgn-np:NP462432.RAgb3OcqDeeer1SA2DP3P2ZB0nal1VQHPDzXWqT-EACFs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP462432.RAgb3OcqDeeer1SA2DP3P2ZB0nal1VQHPDzXWqT-EACFs130_assertion
{
miriam-gene:3021
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN98f2e4e352a5f53cd14d9cb1eeac7523
sio:SIO_000628
miriam-gene:3021
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP462432.RAgb3OcqDeeer1SA2DP3P2ZB0nal1VQHPDzXWqT-EACFs130_provenance
{
dgn-np:NP462432.RAgb3OcqDeeer1SA2DP3P2ZB0nal1VQHPDzXWqT-EACFs130_assertion
dcterms:description
"[Recently, mutations in the ATRX/DAXX chromatin remodeling complex and histone H3.3 were found to correlate with features of ALT in pancreatic neuroendocrine cancers, pediatric glioblastomas, and other tumors of the central nervous system, suggesting that these mutations might contribute to the activation of the ALT pathway in these cancers.]. 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:22829774
;
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:NP462432.RAgb3OcqDeeer1SA2DP3P2ZB0nal1VQHPDzXWqT-EACFs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:35+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" .
}