@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP162914.RA4-FP-mnolX3FM1k8JxICgc0-dSJrDUFfuOlV70a_PqA
> .
@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:NP162914.RA4-FP-mnolX3FM1k8JxICgc0-dSJrDUFfuOlV70a_PqA130_head
{
this:
np:hasAssertion
dgn-np:NP162914.RA4-FP-mnolX3FM1k8JxICgc0-dSJrDUFfuOlV70a_PqA130_assertion
;
np:hasProvenance
dgn-np:NP162914.RA4-FP-mnolX3FM1k8JxICgc0-dSJrDUFfuOlV70a_PqA130_provenance
;
np:hasPublicationInfo
dgn-np:NP162914.RA4-FP-mnolX3FM1k8JxICgc0-dSJrDUFfuOlV70a_PqA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP162914.RA4-FP-mnolX3FM1k8JxICgc0-dSJrDUFfuOlV70a_PqA130_assertion
a
np:Assertion
.
dgn-np:NP162914.RA4-FP-mnolX3FM1k8JxICgc0-dSJrDUFfuOlV70a_PqA130_provenance
a
np:Provenance
.
dgn-np:NP162914.RA4-FP-mnolX3FM1k8JxICgc0-dSJrDUFfuOlV70a_PqA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP162914.RA4-FP-mnolX3FM1k8JxICgc0-dSJrDUFfuOlV70a_PqA130_assertion
{
miriam-gene:3717
a
ncit:C16612
.
lld:C0040028
a
ncit:C7057
.
dgn-gda:DGNc212ff4c2f9c1a093ed5360f70dd1e96
sio:SIO_000628
miriam-gene:3717
,
lld:C0040028
;
a
sio:SIO_001121
.
}
dgn-np:NP162914.RA4-FP-mnolX3FM1k8JxICgc0-dSJrDUFfuOlV70a_PqA130_provenance
{
dgn-np:NP162914.RA4-FP-mnolX3FM1k8JxICgc0-dSJrDUFfuOlV70a_PqA130_assertion
dcterms:description
"[The high prevalence of the V617F mutation of Janus kinase 2 and associated mutations in myeloproliferative disorders (> 95% in polycythemia vera and about half of patients with essential thrombocythemia and primary myelofibrosis) has led the World Health Organization to alter the diagnostic criteria for these myeloproliferative disorders, and these changes are reviewed.]. 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:18300758
;
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:NP162914.RA4-FP-mnolX3FM1k8JxICgc0-dSJrDUFfuOlV70a_PqA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:28+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" .
}