@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP585112.RA-3ZGTFI0QqAxf3LSs8joMnNDjnz0ej-10fAa49gYniE
> .
@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:NP585112.RA-3ZGTFI0QqAxf3LSs8joMnNDjnz0ej-10fAa49gYniE130_head
{
this:
np:hasAssertion
dgn-np:NP585112.RA-3ZGTFI0QqAxf3LSs8joMnNDjnz0ej-10fAa49gYniE130_assertion
;
np:hasProvenance
dgn-np:NP585112.RA-3ZGTFI0QqAxf3LSs8joMnNDjnz0ej-10fAa49gYniE130_provenance
;
np:hasPublicationInfo
dgn-np:NP585112.RA-3ZGTFI0QqAxf3LSs8joMnNDjnz0ej-10fAa49gYniE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP585112.RA-3ZGTFI0QqAxf3LSs8joMnNDjnz0ej-10fAa49gYniE130_assertion
a
np:Assertion
.
dgn-np:NP585112.RA-3ZGTFI0QqAxf3LSs8joMnNDjnz0ej-10fAa49gYniE130_provenance
a
np:Provenance
.
dgn-np:NP585112.RA-3ZGTFI0QqAxf3LSs8joMnNDjnz0ej-10fAa49gYniE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP585112.RA-3ZGTFI0QqAxf3LSs8joMnNDjnz0ej-10fAa49gYniE130_assertion
{
miriam-gene:2241
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGNda9648f62df1c12e0c768e2b5831be12
sio:SIO_000628
miriam-gene:2241
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP585112.RA-3ZGTFI0QqAxf3LSs8joMnNDjnz0ej-10fAa49gYniE130_provenance
{
dgn-np:NP585112.RA-3ZGTFI0QqAxf3LSs8joMnNDjnz0ej-10fAa49gYniE130_assertion
dcterms:description
"[In this study, we analysed the prognostic relevance of foetal liver tyrosine kinase 3 (FLT3) mutations in 73 patients with acute myeloid leukaemia (AML) with normal karyotype, who survived induction and consolidation and received autologous stem cell transplantation (ASCT) after successful mobilization of peripheral blood stem cell (PBSC).]. 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:17036374
;
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:NP585112.RA-3ZGTFI0QqAxf3LSs8joMnNDjnz0ej-10fAa49gYniE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:52+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" .
}