@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP864668.RARMktOCFcKc0reQKhZXElhmc6VM440mJfczqL2pz4D20
> .
@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:NP864668.RARMktOCFcKc0reQKhZXElhmc6VM440mJfczqL2pz4D20130_head
{
this:
np:hasAssertion
dgn-np:NP864668.RARMktOCFcKc0reQKhZXElhmc6VM440mJfczqL2pz4D20130_assertion
;
np:hasProvenance
dgn-np:NP864668.RARMktOCFcKc0reQKhZXElhmc6VM440mJfczqL2pz4D20130_provenance
;
np:hasPublicationInfo
dgn-np:NP864668.RARMktOCFcKc0reQKhZXElhmc6VM440mJfczqL2pz4D20130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP864668.RARMktOCFcKc0reQKhZXElhmc6VM440mJfczqL2pz4D20130_assertion
a
np:Assertion
.
dgn-np:NP864668.RARMktOCFcKc0reQKhZXElhmc6VM440mJfczqL2pz4D20130_provenance
a
np:Provenance
.
dgn-np:NP864668.RARMktOCFcKc0reQKhZXElhmc6VM440mJfczqL2pz4D20130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP864668.RARMktOCFcKc0reQKhZXElhmc6VM440mJfczqL2pz4D20130_assertion
{
miriam-gene:355
a
ncit:C16612
.
lld:C0032463
a
ncit:C7057
.
dgn-gda:DGN3fdf7565b76b7a51208348370be26c64
sio:SIO_000628
miriam-gene:355
,
lld:C0032463
;
a
sio:SIO_001121
.
}
dgn-np:NP864668.RARMktOCFcKc0reQKhZXElhmc6VM440mJfczqL2pz4D20130_provenance
{
dgn-np:NP864668.RARMktOCFcKc0reQKhZXElhmc6VM440mJfczqL2pz4D20130_assertion
dcterms:description
"[With the use of an in vitro culture system to generate differentiating erythroid cells, we found that erythroblasts derived from patients with PV harboring the JAK2 V617F mutation were able to proliferate and generate higher numbers of mature erythroid cells in the presence of inhibitory signals delivered by CD95 (Fas/Apo-1) and TRAIL receptor stimulation.]. 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:16384930
;
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:NP864668.RARMktOCFcKc0reQKhZXElhmc6VM440mJfczqL2pz4D20130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:48+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" .
}