@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP799440.RAFUQ3_ztF0d8NyP2A6maht_XQ5AMYJO5W27E8T0lFq_M
> .
@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:NP799440.RAFUQ3_ztF0d8NyP2A6maht_XQ5AMYJO5W27E8T0lFq_M130_head
{
this:
np:hasAssertion
dgn-np:NP799440.RAFUQ3_ztF0d8NyP2A6maht_XQ5AMYJO5W27E8T0lFq_M130_assertion
;
np:hasProvenance
dgn-np:NP799440.RAFUQ3_ztF0d8NyP2A6maht_XQ5AMYJO5W27E8T0lFq_M130_provenance
;
np:hasPublicationInfo
dgn-np:NP799440.RAFUQ3_ztF0d8NyP2A6maht_XQ5AMYJO5W27E8T0lFq_M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP799440.RAFUQ3_ztF0d8NyP2A6maht_XQ5AMYJO5W27E8T0lFq_M130_assertion
a
np:Assertion
.
dgn-np:NP799440.RAFUQ3_ztF0d8NyP2A6maht_XQ5AMYJO5W27E8T0lFq_M130_provenance
a
np:Provenance
.
dgn-np:NP799440.RAFUQ3_ztF0d8NyP2A6maht_XQ5AMYJO5W27E8T0lFq_M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP799440.RAFUQ3_ztF0d8NyP2A6maht_XQ5AMYJO5W27E8T0lFq_M130_assertion
{
miriam-gene:3717
a
ncit:C16612
.
lld:C0008626
a
ncit:C7057
.
dgn-gda:DGN8b8732f3f36d092d67bfb00e6fd79b3c
sio:SIO_000628
miriam-gene:3717
,
lld:C0008626
;
a
sio:SIO_001121
.
}
dgn-np:NP799440.RAFUQ3_ztF0d8NyP2A6maht_XQ5AMYJO5W27E8T0lFq_M130_provenance
{
dgn-np:NP799440.RAFUQ3_ztF0d8NyP2A6maht_XQ5AMYJO5W27E8T0lFq_M130_assertion
dcterms:description
"[There was no evidence that JAK2 or TET2 mutations were associated with the type of MPN transformation, whereas the type of cytogenetic abnormalities were strongly linked, perhaps indicating that they play a specific role in the transformation process.]. 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:20629097
;
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:NP799440.RAFUQ3_ztF0d8NyP2A6maht_XQ5AMYJO5W27E8T0lFq_M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:10+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" .
}