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http://rdf.disgenet.org/resource/nanopub/NP971534.RA5WK4KIoGI55bAIZOR9lt1KSzfECREEv7ZilyBqs8Mb0
> .
@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
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;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP971534.RA5WK4KIoGI55bAIZOR9lt1KSzfECREEv7ZilyBqs8Mb0130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP971534.RA5WK4KIoGI55bAIZOR9lt1KSzfECREEv7ZilyBqs8Mb0130_assertion
a
np:Assertion
.
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a
np:Provenance
.
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{
miriam-gene:3717
a
ncit:C16612
.
lld:C0001815
a
ncit:C7057
.
dgn-gda:DGN11242c0e90d5456adec332b4d9a1ea14
sio:SIO_000628
miriam-gene:3717
,
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;
a
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.
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dgn-np:NP971534.RA5WK4KIoGI55bAIZOR9lt1KSzfECREEv7ZilyBqs8Mb0130_provenance
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dgn-np:NP971534.RA5WK4KIoGI55bAIZOR9lt1KSzfECREEv7ZilyBqs8Mb0130_assertion
dcterms:description
"[These changes and the resultant clinical research are discussed in this article where we argue that discovery of the JAK2 V617F mutation has signalled the much delayed change in therapeutic paradigm for myelofibrosis and possibly other MPNs from palliation and allowing us to move closer to, but not yet attain, a cure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
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sio:SIO_000772
miriam-pubmed:22463737
;
prov:wasDerivedFrom
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;
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 .
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dgn-np:NP971534.RA5WK4KIoGI55bAIZOR9lt1KSzfECREEv7ZilyBqs8Mb0130_publicationInfo
{
this:
dcterms:created
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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
;
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<
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
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<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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