@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP559660.RArXLtCNfBe1nRld72HjNoTO12w8wm_xVL9J9t2aVw2SE
> .
@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:NP559660.RArXLtCNfBe1nRld72HjNoTO12w8wm_xVL9J9t2aVw2SE130_head
{
this:
np:hasAssertion
dgn-np:NP559660.RArXLtCNfBe1nRld72HjNoTO12w8wm_xVL9J9t2aVw2SE130_assertion
;
np:hasProvenance
dgn-np:NP559660.RArXLtCNfBe1nRld72HjNoTO12w8wm_xVL9J9t2aVw2SE130_provenance
;
np:hasPublicationInfo
dgn-np:NP559660.RArXLtCNfBe1nRld72HjNoTO12w8wm_xVL9J9t2aVw2SE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP559660.RArXLtCNfBe1nRld72HjNoTO12w8wm_xVL9J9t2aVw2SE130_assertion
a
np:Assertion
.
dgn-np:NP559660.RArXLtCNfBe1nRld72HjNoTO12w8wm_xVL9J9t2aVw2SE130_provenance
a
np:Provenance
.
dgn-np:NP559660.RArXLtCNfBe1nRld72HjNoTO12w8wm_xVL9J9t2aVw2SE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP559660.RArXLtCNfBe1nRld72HjNoTO12w8wm_xVL9J9t2aVw2SE130_assertion
{
miriam-gene:2623
a
ncit:C16612
.
lld:C1834582
a
ncit:C7057
.
dgn-gda:DGNdd812ba0ad5d1ef201af317e21e9123d
sio:SIO_000628
miriam-gene:2623
,
lld:C1834582
;
a
sio:SIO_001121
.
}
dgn-np:NP559660.RArXLtCNfBe1nRld72HjNoTO12w8wm_xVL9J9t2aVw2SE130_provenance
{
dgn-np:NP559660.RArXLtCNfBe1nRld72HjNoTO12w8wm_xVL9J9t2aVw2SE130_assertion
dcterms:description
"[Recently, acquired mutations in the megakaryocytic regulator GATA1 have been found in essentially all cases of acute megakaryoblastic leukemia (AMkL) in children with Down syndrome and in the closely related malignancy transient myeloproliferative disorder.]. 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:16840187
;
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:NP559660.RArXLtCNfBe1nRld72HjNoTO12w8wm_xVL9J9t2aVw2SE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:58+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" .
}