@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP440370.RAucU5547CAhnQTqu_LWwUH2MfvJuad-5XYDplYZE9YM8
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP440370.RAucU5547CAhnQTqu_LWwUH2MfvJuad-5XYDplYZE9YM8130_assertion
;
np:hasProvenance
dgn-np:NP440370.RAucU5547CAhnQTqu_LWwUH2MfvJuad-5XYDplYZE9YM8130_provenance
;
np:hasPublicationInfo
dgn-np:NP440370.RAucU5547CAhnQTqu_LWwUH2MfvJuad-5XYDplYZE9YM8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP440370.RAucU5547CAhnQTqu_LWwUH2MfvJuad-5XYDplYZE9YM8130_assertion
a
np:Assertion
.
dgn-np:NP440370.RAucU5547CAhnQTqu_LWwUH2MfvJuad-5XYDplYZE9YM8130_provenance
a
np:Provenance
.
dgn-np:NP440370.RAucU5547CAhnQTqu_LWwUH2MfvJuad-5XYDplYZE9YM8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP440370.RAucU5547CAhnQTqu_LWwUH2MfvJuad-5XYDplYZE9YM8130_assertion
{
miriam-gene:4869
a
ncit:C16612
.
lld:C0220621
a
ncit:C7057
.
dgn-gda:DGNa2fd4e39ee3beb8c4895e09ed7735a20
sio:SIO_000628
miriam-gene:4869
,
lld:C0220621
;
a
sio:SIO_001121
.
}
dgn-np:NP440370.RAucU5547CAhnQTqu_LWwUH2MfvJuad-5XYDplYZE9YM8130_provenance
{
dgn-np:NP440370.RAucU5547CAhnQTqu_LWwUH2MfvJuad-5XYDplYZE9YM8130_assertion
dcterms:description
"[We conclude that analysis of the mutational status of FLT3 and NPM1 at diagnosis is important for prognostic stratification of patients with pediatric AML and that determination of the BAALC gene expression level can add valuable information.]. 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:21967978
;
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 .
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dgn-np:NP440370.RAucU5547CAhnQTqu_LWwUH2MfvJuad-5XYDplYZE9YM8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:20+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" .
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"v2.1.0" .
}