@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP793532.RA2B-hb8x_gtrrvqzOnWiEmXlZWBFXmColPMjns86HPns
> .
@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/
> .
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{
this:
np:hasAssertion
dgn-np:NP793532.RA2B-hb8x_gtrrvqzOnWiEmXlZWBFXmColPMjns86HPns130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP793532.RA2B-hb8x_gtrrvqzOnWiEmXlZWBFXmColPMjns86HPns130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP793532.RA2B-hb8x_gtrrvqzOnWiEmXlZWBFXmColPMjns86HPns130_assertion
a
np:Assertion
.
dgn-np:NP793532.RA2B-hb8x_gtrrvqzOnWiEmXlZWBFXmColPMjns86HPns130_provenance
a
np:Provenance
.
dgn-np:NP793532.RA2B-hb8x_gtrrvqzOnWiEmXlZWBFXmColPMjns86HPns130_publicationInfo
a
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.
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dgn-np:NP793532.RA2B-hb8x_gtrrvqzOnWiEmXlZWBFXmColPMjns86HPns130_assertion
{
miriam-gene:3717
a
ncit:C16612
.
lld:C0033027
a
ncit:C7057
.
dgn-gda:DGNdafbf5b6179f1cfc10d41c652ac1460c
sio:SIO_000628
miriam-gene:3717
,
lld:C0033027
;
a
sio:SIO_001122
.
}
dgn-np:NP793532.RA2B-hb8x_gtrrvqzOnWiEmXlZWBFXmColPMjns86HPns130_provenance
{
dgn-np:NP793532.RA2B-hb8x_gtrrvqzOnWiEmXlZWBFXmColPMjns86HPns130_assertion
dcterms:description
"[To determine if JAK2 V617F mutation is implicated in the abnormal thrombopoiesis of the 3q21q26 syndrome, we analyzed bone marrow samples of 12 patients, including 10 patients with acute myeloid leukemia and 2 patients with a myelodysplastic syndrome, associated with either inv(3)(q21;q26) or t(3;3)(q21;q26).]. 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:20153505
;
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:NP793532.RA2B-hb8x_gtrrvqzOnWiEmXlZWBFXmColPMjns86HPns130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:45+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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;
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
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pav:version
"v4.0.0" .
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