@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP888251.RA2AXoSO84JvxKE54dNomy6eg2wzfSwLVbHbLxy_tnpaI
> .
@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/
> .
dgn-np:NP888251.RA2AXoSO84JvxKE54dNomy6eg2wzfSwLVbHbLxy_tnpaI130_head
{
this:
np:hasAssertion
dgn-np:NP888251.RA2AXoSO84JvxKE54dNomy6eg2wzfSwLVbHbLxy_tnpaI130_assertion
;
np:hasProvenance
dgn-np:NP888251.RA2AXoSO84JvxKE54dNomy6eg2wzfSwLVbHbLxy_tnpaI130_provenance
;
np:hasPublicationInfo
dgn-np:NP888251.RA2AXoSO84JvxKE54dNomy6eg2wzfSwLVbHbLxy_tnpaI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP888251.RA2AXoSO84JvxKE54dNomy6eg2wzfSwLVbHbLxy_tnpaI130_assertion
a
np:Assertion
.
dgn-np:NP888251.RA2AXoSO84JvxKE54dNomy6eg2wzfSwLVbHbLxy_tnpaI130_provenance
a
np:Provenance
.
dgn-np:NP888251.RA2AXoSO84JvxKE54dNomy6eg2wzfSwLVbHbLxy_tnpaI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP888251.RA2AXoSO84JvxKE54dNomy6eg2wzfSwLVbHbLxy_tnpaI130_assertion
{
miriam-gene:4869
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGNffd0ed69bc2802dd579f769b331298bf
sio:SIO_000628
miriam-gene:4869
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP888251.RA2AXoSO84JvxKE54dNomy6eg2wzfSwLVbHbLxy_tnpaI130_provenance
{
dgn-np:NP888251.RA2AXoSO84JvxKE54dNomy6eg2wzfSwLVbHbLxy_tnpaI130_assertion
dcterms:description
"[Mutations of the WT1 gene have been reported as the most common abnormality after NPM1 and FLT3 gene mutations in acute myeloid leukemia (AML), while KIT mutations are predominantly found in core-binding factor (CBF) AMLs.]. 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:21504297
;
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:NP888251.RA2AXoSO84JvxKE54dNomy6eg2wzfSwLVbHbLxy_tnpaI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:27+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}