@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP486893.RAjQjDa_fI4wBLf1noRX5564970eaHlCXD25o37QnVazw
> .
@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:NP486893.RAjQjDa_fI4wBLf1noRX5564970eaHlCXD25o37QnVazw130_head
{
this:
np:hasAssertion
dgn-np:NP486893.RAjQjDa_fI4wBLf1noRX5564970eaHlCXD25o37QnVazw130_assertion
;
np:hasProvenance
dgn-np:NP486893.RAjQjDa_fI4wBLf1noRX5564970eaHlCXD25o37QnVazw130_provenance
;
np:hasPublicationInfo
dgn-np:NP486893.RAjQjDa_fI4wBLf1noRX5564970eaHlCXD25o37QnVazw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP486893.RAjQjDa_fI4wBLf1noRX5564970eaHlCXD25o37QnVazw130_assertion
a
np:Assertion
.
dgn-np:NP486893.RAjQjDa_fI4wBLf1noRX5564970eaHlCXD25o37QnVazw130_provenance
a
np:Provenance
.
dgn-np:NP486893.RAjQjDa_fI4wBLf1noRX5564970eaHlCXD25o37QnVazw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP486893.RAjQjDa_fI4wBLf1noRX5564970eaHlCXD25o37QnVazw130_assertion
{
miriam-gene:6646
a
ncit:C16612
.
lld:C0598766
a
ncit:C7057
.
dgn-gda:DGN6eca803f3af023afc8f7f842b67da6b3
sio:SIO_000628
miriam-gene:6646
,
lld:C0598766
;
a
sio:SIO_001121
.
}
dgn-np:NP486893.RAjQjDa_fI4wBLf1noRX5564970eaHlCXD25o37QnVazw130_provenance
{
dgn-np:NP486893.RAjQjDa_fI4wBLf1noRX5564970eaHlCXD25o37QnVazw130_assertion
dcterms:description
"[Our findings stress that despite the rarity of activating JAK2 mutations in lymphomas, JAK2 is recurrently targeted by numerical, and rarely by structural, genetic aberrations in distinct lymphoma subtypes and that JAK2-STAT pathway may play a role in lymphomagenesis.]. 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:19136931
;
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:NP486893.RAjQjDa_fI4wBLf1noRX5564970eaHlCXD25o37QnVazw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:51+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" .
}