@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP552129.RAg9mhjNtdrYAbZNKXeQvD2NDChAQel2gkE_hq8iaztlI
> .
@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:NP552129.RAg9mhjNtdrYAbZNKXeQvD2NDChAQel2gkE_hq8iaztlI130_head
{
this:
np:hasAssertion
dgn-np:NP552129.RAg9mhjNtdrYAbZNKXeQvD2NDChAQel2gkE_hq8iaztlI130_assertion
;
np:hasProvenance
dgn-np:NP552129.RAg9mhjNtdrYAbZNKXeQvD2NDChAQel2gkE_hq8iaztlI130_provenance
;
np:hasPublicationInfo
dgn-np:NP552129.RAg9mhjNtdrYAbZNKXeQvD2NDChAQel2gkE_hq8iaztlI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP552129.RAg9mhjNtdrYAbZNKXeQvD2NDChAQel2gkE_hq8iaztlI130_assertion
a
np:Assertion
.
dgn-np:NP552129.RAg9mhjNtdrYAbZNKXeQvD2NDChAQel2gkE_hq8iaztlI130_provenance
a
np:Provenance
.
dgn-np:NP552129.RAg9mhjNtdrYAbZNKXeQvD2NDChAQel2gkE_hq8iaztlI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP552129.RAg9mhjNtdrYAbZNKXeQvD2NDChAQel2gkE_hq8iaztlI130_assertion
{
miriam-gene:7083
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGNdacc67e27bfde6586c6d507e6b24373d
sio:SIO_000628
miriam-gene:7083
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP552129.RAg9mhjNtdrYAbZNKXeQvD2NDChAQel2gkE_hq8iaztlI130_provenance
{
dgn-np:NP552129.RAg9mhjNtdrYAbZNKXeQvD2NDChAQel2gkE_hq8iaztlI130_assertion
dcterms:description
"[Gain-of-function mutations in the second intracellular kinase domain (TK2) and in the juxtamembrane domain are described in patients with core binding factor acute myeloid leukemia (CBFL) and are associated with leukocytosis.]. 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:15339674
;
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:NP552129.RAg9mhjNtdrYAbZNKXeQvD2NDChAQel2gkE_hq8iaztlI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:33+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" .
}