@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP455526.RAiQ1jwYigAh9XOwM9gtUu_8H44Wg1xtQlKThU7nMks5A
> .
@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:NP455526.RAiQ1jwYigAh9XOwM9gtUu_8H44Wg1xtQlKThU7nMks5A130_head
{
this:
np:hasAssertion
dgn-np:NP455526.RAiQ1jwYigAh9XOwM9gtUu_8H44Wg1xtQlKThU7nMks5A130_assertion
;
np:hasProvenance
dgn-np:NP455526.RAiQ1jwYigAh9XOwM9gtUu_8H44Wg1xtQlKThU7nMks5A130_provenance
;
np:hasPublicationInfo
dgn-np:NP455526.RAiQ1jwYigAh9XOwM9gtUu_8H44Wg1xtQlKThU7nMks5A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP455526.RAiQ1jwYigAh9XOwM9gtUu_8H44Wg1xtQlKThU7nMks5A130_assertion
a
np:Assertion
.
dgn-np:NP455526.RAiQ1jwYigAh9XOwM9gtUu_8H44Wg1xtQlKThU7nMks5A130_provenance
a
np:Provenance
.
dgn-np:NP455526.RAiQ1jwYigAh9XOwM9gtUu_8H44Wg1xtQlKThU7nMks5A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP455526.RAiQ1jwYigAh9XOwM9gtUu_8H44Wg1xtQlKThU7nMks5A130_assertion
{
miriam-gene:2623
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNb5fea86b1a5e9c15726bf334335957bb
sio:SIO_000628
miriam-gene:2623
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP455526.RAiQ1jwYigAh9XOwM9gtUu_8H44Wg1xtQlKThU7nMks5A130_provenance
{
dgn-np:NP455526.RAiQ1jwYigAh9XOwM9gtUu_8H44Wg1xtQlKThU7nMks5A130_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-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:NP455526.RAiQ1jwYigAh9XOwM9gtUu_8H44Wg1xtQlKThU7nMks5A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:31+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" .
}