@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP254953.RAKhvMfOrJCCKpSErKQFhqgxo-5nBwiXEngiwYRQmFdYE
> .
@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:NP254953.RAKhvMfOrJCCKpSErKQFhqgxo-5nBwiXEngiwYRQmFdYE130_head
{
this:
np:hasAssertion
dgn-np:NP254953.RAKhvMfOrJCCKpSErKQFhqgxo-5nBwiXEngiwYRQmFdYE130_assertion
;
np:hasProvenance
dgn-np:NP254953.RAKhvMfOrJCCKpSErKQFhqgxo-5nBwiXEngiwYRQmFdYE130_provenance
;
np:hasPublicationInfo
dgn-np:NP254953.RAKhvMfOrJCCKpSErKQFhqgxo-5nBwiXEngiwYRQmFdYE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP254953.RAKhvMfOrJCCKpSErKQFhqgxo-5nBwiXEngiwYRQmFdYE130_assertion
a
np:Assertion
.
dgn-np:NP254953.RAKhvMfOrJCCKpSErKQFhqgxo-5nBwiXEngiwYRQmFdYE130_provenance
a
np:Provenance
.
dgn-np:NP254953.RAKhvMfOrJCCKpSErKQFhqgxo-5nBwiXEngiwYRQmFdYE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP254953.RAKhvMfOrJCCKpSErKQFhqgxo-5nBwiXEngiwYRQmFdYE130_assertion
{
miriam-gene:10320
a
ncit:C16612
.
lld:C1961102
a
ncit:C7057
.
dgn-gda:DGN08b753db44e02cd41f8df7bfbdc35fea
sio:SIO_000628
miriam-gene:10320
,
lld:C1961102
;
a
sio:SIO_001121
.
}
dgn-np:NP254953.RAKhvMfOrJCCKpSErKQFhqgxo-5nBwiXEngiwYRQmFdYE130_provenance
{
dgn-np:NP254953.RAKhvMfOrJCCKpSErKQFhqgxo-5nBwiXEngiwYRQmFdYE130_assertion
dcterms:description
"[High-resolution genomic profiling of genetic alterations and gene expression has revolutionized our understanding of the genetic basis of ALL, and has identified several alterations associated with poor outcome, including mutations of the lymphoid transcription factor gene IKZF1 (IKAROS), activating mutations of Janus kinases, and rearrangement of the lymphoid cytokine receptor gene CRLF2.]. 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:21370430
;
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:NP254953.RAKhvMfOrJCCKpSErKQFhqgxo-5nBwiXEngiwYRQmFdYE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:22+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" .
}