@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP591321.RA4El39y5rXOWJJltwXHt4HY8nlmEHDzAut5OskKnsl8M
> .
@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:NP591321.RA4El39y5rXOWJJltwXHt4HY8nlmEHDzAut5OskKnsl8M130_head
{
this:
np:hasAssertion
dgn-np:NP591321.RA4El39y5rXOWJJltwXHt4HY8nlmEHDzAut5OskKnsl8M130_assertion
;
np:hasProvenance
dgn-np:NP591321.RA4El39y5rXOWJJltwXHt4HY8nlmEHDzAut5OskKnsl8M130_provenance
;
np:hasPublicationInfo
dgn-np:NP591321.RA4El39y5rXOWJJltwXHt4HY8nlmEHDzAut5OskKnsl8M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP591321.RA4El39y5rXOWJJltwXHt4HY8nlmEHDzAut5OskKnsl8M130_assertion
a
np:Assertion
.
dgn-np:NP591321.RA4El39y5rXOWJJltwXHt4HY8nlmEHDzAut5OskKnsl8M130_provenance
a
np:Provenance
.
dgn-np:NP591321.RA4El39y5rXOWJJltwXHt4HY8nlmEHDzAut5OskKnsl8M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP591321.RA4El39y5rXOWJJltwXHt4HY8nlmEHDzAut5OskKnsl8M130_assertion
{
miriam-gene:1788
a
ncit:C16612
.
lld:C0023487
a
ncit:C7057
.
dgn-gda:DGN0d44ab8b5aeccd9abd4810f2bb23973c
sio:SIO_000628
miriam-gene:1788
,
lld:C0023487
;
a
sio:SIO_001121
.
}
dgn-np:NP591321.RA4El39y5rXOWJJltwXHt4HY8nlmEHDzAut5OskKnsl8M130_provenance
{
dgn-np:NP591321.RA4El39y5rXOWJJltwXHt4HY8nlmEHDzAut5OskKnsl8M130_assertion
dcterms:description
"[To assess their prognostic significance, we determined the mutational status of DNMT3A exon 23 in 288 patients with AML excluding acute promyelocytic leukemia, aged from 18 to 65 years and treated in Toulouse University Hospital.]. 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:22081665
;
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:NP591321.RA4El39y5rXOWJJltwXHt4HY8nlmEHDzAut5OskKnsl8M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:55+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" .
}