@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP323197.RAltkI5-ITvrWVQEoPTjzL4_HfpyCSSUOnDvuOrac6xKk
> .
@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:NP323197.RAltkI5-ITvrWVQEoPTjzL4_HfpyCSSUOnDvuOrac6xKk130_head
{
this:
np:hasAssertion
dgn-np:NP323197.RAltkI5-ITvrWVQEoPTjzL4_HfpyCSSUOnDvuOrac6xKk130_assertion
;
np:hasProvenance
dgn-np:NP323197.RAltkI5-ITvrWVQEoPTjzL4_HfpyCSSUOnDvuOrac6xKk130_provenance
;
np:hasPublicationInfo
dgn-np:NP323197.RAltkI5-ITvrWVQEoPTjzL4_HfpyCSSUOnDvuOrac6xKk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP323197.RAltkI5-ITvrWVQEoPTjzL4_HfpyCSSUOnDvuOrac6xKk130_assertion
a
np:Assertion
.
dgn-np:NP323197.RAltkI5-ITvrWVQEoPTjzL4_HfpyCSSUOnDvuOrac6xKk130_provenance
a
np:Provenance
.
dgn-np:NP323197.RAltkI5-ITvrWVQEoPTjzL4_HfpyCSSUOnDvuOrac6xKk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP323197.RAltkI5-ITvrWVQEoPTjzL4_HfpyCSSUOnDvuOrac6xKk130_assertion
{
miriam-gene:3717
a
ncit:C16612
.
lld:C0836924
a
ncit:C7057
.
dgn-gda:DGN2a720be8214a9afec845806db5c9119f
sio:SIO_000628
miriam-gene:3717
,
lld:C0836924
;
a
sio:SIO_001121
.
}
dgn-np:NP323197.RAltkI5-ITvrWVQEoPTjzL4_HfpyCSSUOnDvuOrac6xKk130_provenance
{
dgn-np:NP323197.RAltkI5-ITvrWVQEoPTjzL4_HfpyCSSUOnDvuOrac6xKk130_assertion
dcterms:description
"[The lack of thrombocytosis suggests that additional events may be required for JAK2 V617F to cause ET, but qualitative platelet abnormalities induced by JAK2 V617F may contribute to the hemostatic complications of PV.]. 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:17183644
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP323197.RAltkI5-ITvrWVQEoPTjzL4_HfpyCSSUOnDvuOrac6xKk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:09+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" .
}