@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP68771.RAD_xwNKhs7Vaez-X_CUoOwRyfywPO97oZV5YFxKBgFCc
> .
@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:NP68771.RAD_xwNKhs7Vaez-X_CUoOwRyfywPO97oZV5YFxKBgFCc130_head
{
this:
np:hasAssertion
dgn-np:NP68771.RAD_xwNKhs7Vaez-X_CUoOwRyfywPO97oZV5YFxKBgFCc130_assertion
;
np:hasProvenance
dgn-np:NP68771.RAD_xwNKhs7Vaez-X_CUoOwRyfywPO97oZV5YFxKBgFCc130_provenance
;
np:hasPublicationInfo
dgn-np:NP68771.RAD_xwNKhs7Vaez-X_CUoOwRyfywPO97oZV5YFxKBgFCc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP68771.RAD_xwNKhs7Vaez-X_CUoOwRyfywPO97oZV5YFxKBgFCc130_assertion
a
np:Assertion
.
dgn-np:NP68771.RAD_xwNKhs7Vaez-X_CUoOwRyfywPO97oZV5YFxKBgFCc130_provenance
a
np:Provenance
.
dgn-np:NP68771.RAD_xwNKhs7Vaez-X_CUoOwRyfywPO97oZV5YFxKBgFCc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP68771.RAD_xwNKhs7Vaez-X_CUoOwRyfywPO97oZV5YFxKBgFCc130_assertion
{
miriam-gene:4893
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN45f4cb96d225b6d1143f15c19f7e0bed
sio:SIO_000628
miriam-gene:4893
,
lld:C0023467
;
a
sio:SIO_001122
.
}
dgn-np:NP68771.RAD_xwNKhs7Vaez-X_CUoOwRyfywPO97oZV5YFxKBgFCc130_provenance
{
dgn-np:NP68771.RAD_xwNKhs7Vaez-X_CUoOwRyfywPO97oZV5YFxKBgFCc130_assertion
dcterms:description
"[We compared the mutational status of the NPM1, FLT3, CEBPA, MLL, and NRAS genes in leukemia cells with the clinical outcome in 872 adults younger than 60 years of age with cytogenetically normal AML.]. 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:18450602
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP68771.RAD_xwNKhs7Vaez-X_CUoOwRyfywPO97oZV5YFxKBgFCc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:33+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
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"v2.1.0" .
}