@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP852944.RAN7L_7K0iLoo3Pa6EKXL787xM4eDD524jpTNK2w5qqrg
> .
@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:NP852944.RAN7L_7K0iLoo3Pa6EKXL787xM4eDD524jpTNK2w5qqrg130_head
{
this:
np:hasAssertion
dgn-np:NP852944.RAN7L_7K0iLoo3Pa6EKXL787xM4eDD524jpTNK2w5qqrg130_assertion
;
np:hasProvenance
dgn-np:NP852944.RAN7L_7K0iLoo3Pa6EKXL787xM4eDD524jpTNK2w5qqrg130_provenance
;
np:hasPublicationInfo
dgn-np:NP852944.RAN7L_7K0iLoo3Pa6EKXL787xM4eDD524jpTNK2w5qqrg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP852944.RAN7L_7K0iLoo3Pa6EKXL787xM4eDD524jpTNK2w5qqrg130_assertion
a
np:Assertion
.
dgn-np:NP852944.RAN7L_7K0iLoo3Pa6EKXL787xM4eDD524jpTNK2w5qqrg130_provenance
a
np:Provenance
.
dgn-np:NP852944.RAN7L_7K0iLoo3Pa6EKXL787xM4eDD524jpTNK2w5qqrg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP852944.RAN7L_7K0iLoo3Pa6EKXL787xM4eDD524jpTNK2w5qqrg130_assertion
{
miriam-gene:2623
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN834a831dd8037524873e2e1280a335f7
sio:SIO_000628
miriam-gene:2623
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP852944.RAN7L_7K0iLoo3Pa6EKXL787xM4eDD524jpTNK2w5qqrg130_provenance
{
dgn-np:NP852944.RAN7L_7K0iLoo3Pa6EKXL787xM4eDD524jpTNK2w5qqrg130_assertion
dcterms:description
"[Notable among DS children with acute myeloid leukemia (AML), is the high frequency of the acute megakaryocytic leukemia (AMkL) subtype, which uniformly harbor somatic mutations in the transcription factor GATA1 gene.]. 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:21083461
;
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:NP852944.RAN7L_7K0iLoo3Pa6EKXL787xM4eDD524jpTNK2w5qqrg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:11+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" .
}