@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP233772.RApE19b3H3_IGdTikwvI5WTD2K_DTLBuZ4e7OdGIFKW9U
> .
@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:NP233772.RApE19b3H3_IGdTikwvI5WTD2K_DTLBuZ4e7OdGIFKW9U130_head
{
this:
np:hasAssertion
dgn-np:NP233772.RApE19b3H3_IGdTikwvI5WTD2K_DTLBuZ4e7OdGIFKW9U130_assertion
;
np:hasProvenance
dgn-np:NP233772.RApE19b3H3_IGdTikwvI5WTD2K_DTLBuZ4e7OdGIFKW9U130_provenance
;
np:hasPublicationInfo
dgn-np:NP233772.RApE19b3H3_IGdTikwvI5WTD2K_DTLBuZ4e7OdGIFKW9U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP233772.RApE19b3H3_IGdTikwvI5WTD2K_DTLBuZ4e7OdGIFKW9U130_assertion
a
np:Assertion
.
dgn-np:NP233772.RApE19b3H3_IGdTikwvI5WTD2K_DTLBuZ4e7OdGIFKW9U130_provenance
a
np:Provenance
.
dgn-np:NP233772.RApE19b3H3_IGdTikwvI5WTD2K_DTLBuZ4e7OdGIFKW9U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP233772.RApE19b3H3_IGdTikwvI5WTD2K_DTLBuZ4e7OdGIFKW9U130_assertion
{
miriam-gene:3717
a
ncit:C16612
.
lld:C0026987
a
ncit:C7057
.
dgn-gda:DGNbbb3d8c186085f6c2d44bd5c877331e3
sio:SIO_000628
miriam-gene:3717
,
lld:C0026987
;
a
sio:SIO_001121
.
}
dgn-np:NP233772.RApE19b3H3_IGdTikwvI5WTD2K_DTLBuZ4e7OdGIFKW9U130_provenance
{
dgn-np:NP233772.RApE19b3H3_IGdTikwvI5WTD2K_DTLBuZ4e7OdGIFKW9U130_assertion
dcterms:description
"[A somatic activating mutation (V617F) in the JAK2 tyrosine kinase was recently discovered in the majority of patients with polycythemia vera (PV), and some with essential thrombocythemia (ET) and chronic idiopathic 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: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:NP233772.RApE19b3H3_IGdTikwvI5WTD2K_DTLBuZ4e7OdGIFKW9U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:11+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" .
}