@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1026352.RAjoRDG_iUF70jB90dFrWBxYHJvGsAWAa5thLTu7oJ8sI
> .
@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:NP1026352.RAjoRDG_iUF70jB90dFrWBxYHJvGsAWAa5thLTu7oJ8sI130_head
{
this:
np:hasAssertion
dgn-np:NP1026352.RAjoRDG_iUF70jB90dFrWBxYHJvGsAWAa5thLTu7oJ8sI130_assertion
;
np:hasProvenance
dgn-np:NP1026352.RAjoRDG_iUF70jB90dFrWBxYHJvGsAWAa5thLTu7oJ8sI130_provenance
;
np:hasPublicationInfo
dgn-np:NP1026352.RAjoRDG_iUF70jB90dFrWBxYHJvGsAWAa5thLTu7oJ8sI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1026352.RAjoRDG_iUF70jB90dFrWBxYHJvGsAWAa5thLTu7oJ8sI130_assertion
a
np:Assertion
.
dgn-np:NP1026352.RAjoRDG_iUF70jB90dFrWBxYHJvGsAWAa5thLTu7oJ8sI130_provenance
a
np:Provenance
.
dgn-np:NP1026352.RAjoRDG_iUF70jB90dFrWBxYHJvGsAWAa5thLTu7oJ8sI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1026352.RAjoRDG_iUF70jB90dFrWBxYHJvGsAWAa5thLTu7oJ8sI130_assertion
{
miriam-gene:3717
a
ncit:C16612
.
lld:C0026987
a
ncit:C7057
.
dgn-gda:DGN50076c2d4b5f091daefb1b0db67602e0
sio:SIO_000628
miriam-gene:3717
,
lld:C0026987
;
a
sio:SIO_001122
.
}
dgn-np:NP1026352.RAjoRDG_iUF70jB90dFrWBxYHJvGsAWAa5thLTu7oJ8sI130_provenance
{
dgn-np:NP1026352.RAjoRDG_iUF70jB90dFrWBxYHJvGsAWAa5thLTu7oJ8sI130_assertion
dcterms:description
"[The JAK2 V617F mutational status and its allele burden correlate with the clinicohematologic phenotypes of ET patients, including older age, higher neutrophil count, and greater rates of organomegaly, thrombotic events, and myelofibrosis.]. 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:23130336
;
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:NP1026352.RAjoRDG_iUF70jB90dFrWBxYHJvGsAWAa5thLTu7oJ8sI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:31+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" .
}