@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1359498.RAXigP5_d9oNOmc0vtZeNjRoF0wM5CoqQl0NJ-JMquKCE
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
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{
this:
np:hasAssertion
dgn-np:NP1359498.RAXigP5_d9oNOmc0vtZeNjRoF0wM5CoqQl0NJ-JMquKCE130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
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a
np:Nanopublication
.
dgn-np:NP1359498.RAXigP5_d9oNOmc0vtZeNjRoF0wM5CoqQl0NJ-JMquKCE130_assertion
a
np:Assertion
.
dgn-np:NP1359498.RAXigP5_d9oNOmc0vtZeNjRoF0wM5CoqQl0NJ-JMquKCE130_provenance
a
np:Provenance
.
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a
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.
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{
miriam-gene:865
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGNdef4286e3886ec3f7e16665f93950c2d
sio:SIO_000628
miriam-gene:865
,
lld:C0023467
;
a
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.
}
dgn-np:NP1359498.RAXigP5_d9oNOmc0vtZeNjRoF0wM5CoqQl0NJ-JMquKCE130_provenance
{
dgn-np:NP1359498.RAXigP5_d9oNOmc0vtZeNjRoF0wM5CoqQl0NJ-JMquKCE130_assertion
dcterms:description
"[We conclude that CBFB/MYH11 fusion transcript detection, as a surrogate for the favorable prognosis and treatment planning implied by inv(16) in AML M4Eo, should not be exclusively relied upon in AML M1 in the absence of prospective study of this specific (M1) category of AML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:8847901
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1359498.RAXigP5_d9oNOmc0vtZeNjRoF0wM5CoqQl0NJ-JMquKCE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:02+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
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;
pav:authoredBy
<
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> , <
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> , <
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
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