@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP600795.RA_frcnUSIin_XiNmN2CqHGflpMTx2ZZRNnBJtHjS8ktY
> .
@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:NP600795.RA_frcnUSIin_XiNmN2CqHGflpMTx2ZZRNnBJtHjS8ktY130_head
{
this:
np:hasAssertion
dgn-np:NP600795.RA_frcnUSIin_XiNmN2CqHGflpMTx2ZZRNnBJtHjS8ktY130_assertion
;
np:hasProvenance
dgn-np:NP600795.RA_frcnUSIin_XiNmN2CqHGflpMTx2ZZRNnBJtHjS8ktY130_provenance
;
np:hasPublicationInfo
dgn-np:NP600795.RA_frcnUSIin_XiNmN2CqHGflpMTx2ZZRNnBJtHjS8ktY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP600795.RA_frcnUSIin_XiNmN2CqHGflpMTx2ZZRNnBJtHjS8ktY130_assertion
a
np:Assertion
.
dgn-np:NP600795.RA_frcnUSIin_XiNmN2CqHGflpMTx2ZZRNnBJtHjS8ktY130_provenance
a
np:Provenance
.
dgn-np:NP600795.RA_frcnUSIin_XiNmN2CqHGflpMTx2ZZRNnBJtHjS8ktY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP600795.RA_frcnUSIin_XiNmN2CqHGflpMTx2ZZRNnBJtHjS8ktY130_assertion
{
miriam-gene:1440
a
ncit:C16612
.
lld:C0032463
a
ncit:C7057
.
dgn-gda:DGN1ebc500cb12983acd97af8d0cccb2270
sio:SIO_000628
miriam-gene:1440
,
lld:C0032463
;
a
sio:SIO_001121
.
}
dgn-np:NP600795.RA_frcnUSIin_XiNmN2CqHGflpMTx2ZZRNnBJtHjS8ktY130_provenance
{
dgn-np:NP600795.RA_frcnUSIin_XiNmN2CqHGflpMTx2ZZRNnBJtHjS8ktY130_assertion
dcterms:description
"[Since the V617F mutation in JAK2 may not be the initiating event in myeloprofilerative disorders (MPDs) we compared molecular changes in neutrophils from patients with polycythemia vera (PV) and essential thrombocythosis (ET), to neutrophils stimulated by G-CSF administration and to normal unstimulated neutrophils]. 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:19497108
;
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:NP600795.RA_frcnUSIin_XiNmN2CqHGflpMTx2ZZRNnBJtHjS8ktY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:01+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" .
}