@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP240438.RAF7e16aY_9NhBncQY_zuwE-UfzquvLOJvanHDJzlgJi0
> .
@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:NP240438.RAF7e16aY_9NhBncQY_zuwE-UfzquvLOJvanHDJzlgJi0130_head
{
this:
np:hasAssertion
dgn-np:NP240438.RAF7e16aY_9NhBncQY_zuwE-UfzquvLOJvanHDJzlgJi0130_assertion
;
np:hasProvenance
dgn-np:NP240438.RAF7e16aY_9NhBncQY_zuwE-UfzquvLOJvanHDJzlgJi0130_provenance
;
np:hasPublicationInfo
dgn-np:NP240438.RAF7e16aY_9NhBncQY_zuwE-UfzquvLOJvanHDJzlgJi0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP240438.RAF7e16aY_9NhBncQY_zuwE-UfzquvLOJvanHDJzlgJi0130_assertion
a
np:Assertion
.
dgn-np:NP240438.RAF7e16aY_9NhBncQY_zuwE-UfzquvLOJvanHDJzlgJi0130_provenance
a
np:Provenance
.
dgn-np:NP240438.RAF7e16aY_9NhBncQY_zuwE-UfzquvLOJvanHDJzlgJi0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP240438.RAF7e16aY_9NhBncQY_zuwE-UfzquvLOJvanHDJzlgJi0130_assertion
{
miriam-gene:4914
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN6a46674b81d5a31cb15436ba36c86376
sio:SIO_000628
miriam-gene:4914
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP240438.RAF7e16aY_9NhBncQY_zuwE-UfzquvLOJvanHDJzlgJi0130_provenance
{
dgn-np:NP240438.RAF7e16aY_9NhBncQY_zuwE-UfzquvLOJvanHDJzlgJi0130_assertion
dcterms:description
"[We reviewed the frequency and prognostic significance of FLT3 (fms-like tyrosine kinase receptor-3) and NPM (nucleophosmin) gene mutations and WT1 (Wilms' tumor) and BAALC (brain and acute leukemia, cytoplasmic) gene expression in 100 consecutive patients with intermediate and poor cytogenetic risk de novo acute myeloid leukemia (AML) receiving conventional anthracycline-AraC based therapy.]. 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:21942328
;
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:NP240438.RAF7e16aY_9NhBncQY_zuwE-UfzquvLOJvanHDJzlgJi0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:14+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" .
}