@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP20674.RAfYmxKkBWUbHhYmvBZnoprMjk5SWgk2Ac6Hg3iKQExbw
> .
@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:NP20674.RAfYmxKkBWUbHhYmvBZnoprMjk5SWgk2Ac6Hg3iKQExbw130_head
{
this:
np:hasAssertion
dgn-np:NP20674.RAfYmxKkBWUbHhYmvBZnoprMjk5SWgk2Ac6Hg3iKQExbw130_assertion
;
np:hasProvenance
dgn-np:NP20674.RAfYmxKkBWUbHhYmvBZnoprMjk5SWgk2Ac6Hg3iKQExbw130_provenance
;
np:hasPublicationInfo
dgn-np:NP20674.RAfYmxKkBWUbHhYmvBZnoprMjk5SWgk2Ac6Hg3iKQExbw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP20674.RAfYmxKkBWUbHhYmvBZnoprMjk5SWgk2Ac6Hg3iKQExbw130_assertion
a
np:Assertion
.
dgn-np:NP20674.RAfYmxKkBWUbHhYmvBZnoprMjk5SWgk2Ac6Hg3iKQExbw130_provenance
a
np:Provenance
.
dgn-np:NP20674.RAfYmxKkBWUbHhYmvBZnoprMjk5SWgk2Ac6Hg3iKQExbw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP20674.RAfYmxKkBWUbHhYmvBZnoprMjk5SWgk2Ac6Hg3iKQExbw130_assertion
{
miriam-gene:3717
a
ncit:C16612
.
lld:C0836924
a
ncit:C7057
.
dgn-gda:DGN50e534b2d6b732b56c1fd052885ca9a9
sio:SIO_000628
miriam-gene:3717
,
lld:C0836924
;
a
sio:SIO_001121
.
}
dgn-np:NP20674.RAfYmxKkBWUbHhYmvBZnoprMjk5SWgk2Ac6Hg3iKQExbw130_provenance
{
dgn-np:NP20674.RAfYmxKkBWUbHhYmvBZnoprMjk5SWgk2Ac6Hg3iKQExbw130_assertion
dcterms:description
"[Given that the identical somatic activating mutation in the JAK2 tyrosine kinase gene (JAK2(V617F)) is observed in most individuals with polycythemia vera, essential thrombocythemia and primary myelofibrosis, there likely are additional genetic events that contribute to the pathogenesis of these phenotypically distinct disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:19287384
;
prov:wasDerivedFrom
dgn-void:ctd_human-20130708
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20130708
pav:importedOn
"2013-07-24"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP20674.RAfYmxKkBWUbHhYmvBZnoprMjk5SWgk2Ac6Hg3iKQExbw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:08+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" .
}