@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP516816.RAEE_Bx-qWyCkSpGlnKPVlH6XSQoc3nVDyJ5wwf6VekQk
> .
@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/
> .
dgn-np:NP516816.RAEE_Bx-qWyCkSpGlnKPVlH6XSQoc3nVDyJ5wwf6VekQk130_head
{
this:
np:hasAssertion
dgn-np:NP516816.RAEE_Bx-qWyCkSpGlnKPVlH6XSQoc3nVDyJ5wwf6VekQk130_assertion
;
np:hasProvenance
dgn-np:NP516816.RAEE_Bx-qWyCkSpGlnKPVlH6XSQoc3nVDyJ5wwf6VekQk130_provenance
;
np:hasPublicationInfo
dgn-np:NP516816.RAEE_Bx-qWyCkSpGlnKPVlH6XSQoc3nVDyJ5wwf6VekQk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP516816.RAEE_Bx-qWyCkSpGlnKPVlH6XSQoc3nVDyJ5wwf6VekQk130_assertion
a
np:Assertion
.
dgn-np:NP516816.RAEE_Bx-qWyCkSpGlnKPVlH6XSQoc3nVDyJ5wwf6VekQk130_provenance
a
np:Provenance
.
dgn-np:NP516816.RAEE_Bx-qWyCkSpGlnKPVlH6XSQoc3nVDyJ5wwf6VekQk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP516816.RAEE_Bx-qWyCkSpGlnKPVlH6XSQoc3nVDyJ5wwf6VekQk130_assertion
{
miriam-gene:3717
a
ncit:C16612
.
lld:C1292778
a
ncit:C7057
.
dgn-gda:DGN963ee3df7e511a1436a679a2b03cbdda
sio:SIO_000628
miriam-gene:3717
,
lld:C1292778
;
a
sio:SIO_001122
.
}
dgn-np:NP516816.RAEE_Bx-qWyCkSpGlnKPVlH6XSQoc3nVDyJ5wwf6VekQk130_provenance
{
dgn-np:NP516816.RAEE_Bx-qWyCkSpGlnKPVlH6XSQoc3nVDyJ5wwf6VekQk130_assertion
dcterms:description
"[However, it is very clear that some patients with classical PV lack the JAK2 V617F mutation, while some patients with other chronic myeloproliferative disorders such as idiopathic myelofibrosis (IMF) and essential thrombocytosis (ET) also express the JAK2 V617F mutation.]. 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:16210034
;
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:NP516816.RAEE_Bx-qWyCkSpGlnKPVlH6XSQoc3nVDyJ5wwf6VekQk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:39+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}