@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP71499.RARLO0bUZJ8xsisFuhsQi46FqK1r_GdMVNXYJlszf40T4
> .
@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 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:NP71499.RARLO0bUZJ8xsisFuhsQi46FqK1r_GdMVNXYJlszf40T4130_head
{
this:
np:hasAssertion
dgn-np:NP71499.RARLO0bUZJ8xsisFuhsQi46FqK1r_GdMVNXYJlszf40T4130_assertion
;
np:hasProvenance
dgn-np:NP71499.RARLO0bUZJ8xsisFuhsQi46FqK1r_GdMVNXYJlszf40T4130_provenance
;
np:hasPublicationInfo
dgn-np:NP71499.RARLO0bUZJ8xsisFuhsQi46FqK1r_GdMVNXYJlszf40T4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP71499.RARLO0bUZJ8xsisFuhsQi46FqK1r_GdMVNXYJlszf40T4130_assertion
a
np:Assertion
.
dgn-np:NP71499.RARLO0bUZJ8xsisFuhsQi46FqK1r_GdMVNXYJlszf40T4130_provenance
a
np:Provenance
.
dgn-np:NP71499.RARLO0bUZJ8xsisFuhsQi46FqK1r_GdMVNXYJlszf40T4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP71499.RARLO0bUZJ8xsisFuhsQi46FqK1r_GdMVNXYJlszf40T4130_assertion
{
miriam-gene:3717
a
ncit:C16612
.
lld:C0027022
a
ncit:C7057
.
dgn-gda:DGNe65fd3dc319f6cfb48b138813bed0273
sio:SIO_000628
miriam-gene:3717
,
lld:C0027022
;
a
sio:SIO_001122
.
}
dgn-np:NP71499.RARLO0bUZJ8xsisFuhsQi46FqK1r_GdMVNXYJlszf40T4130_provenance
{
dgn-np:NP71499.RARLO0bUZJ8xsisFuhsQi46FqK1r_GdMVNXYJlszf40T4130_assertion
dct: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_literature
;
sio:SIO_000772
miriam-pubmed:19287384
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP71499.RARLO0bUZJ8xsisFuhsQi46FqK1r_GdMVNXYJlszf40T4130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:34+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}