@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP519521.RA2HREzbnCPQMY7QDVMNScaup8X-R4x9ZwIPaGc3BtXkg
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP519521.RA2HREzbnCPQMY7QDVMNScaup8X-R4x9ZwIPaGc3BtXkg130_head
{
this:
np:hasAssertion
dgn-np:NP519521.RA2HREzbnCPQMY7QDVMNScaup8X-R4x9ZwIPaGc3BtXkg130_assertion
;
np:hasProvenance
dgn-np:NP519521.RA2HREzbnCPQMY7QDVMNScaup8X-R4x9ZwIPaGc3BtXkg130_provenance
;
np:hasPublicationInfo
dgn-np:NP519521.RA2HREzbnCPQMY7QDVMNScaup8X-R4x9ZwIPaGc3BtXkg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP519521.RA2HREzbnCPQMY7QDVMNScaup8X-R4x9ZwIPaGc3BtXkg130_assertion
a
np:Assertion
.
dgn-np:NP519521.RA2HREzbnCPQMY7QDVMNScaup8X-R4x9ZwIPaGc3BtXkg130_provenance
a
np:Provenance
.
dgn-np:NP519521.RA2HREzbnCPQMY7QDVMNScaup8X-R4x9ZwIPaGc3BtXkg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP519521.RA2HREzbnCPQMY7QDVMNScaup8X-R4x9ZwIPaGc3BtXkg130_assertion
{
miriam-gene:3717
a
ncit:C16612
.
lld:C0242596
a
ncit:C7057
.
dgn-gda:DGN5336e7bf5254e6d34c8125ce0f8e981a
sio:SIO_000628
miriam-gene:3717
,
lld:C0242596
;
a
sio:SIO_001122
.
}
dgn-np:NP519521.RA2HREzbnCPQMY7QDVMNScaup8X-R4x9ZwIPaGc3BtXkg130_provenance
{
dgn-np:NP519521.RA2HREzbnCPQMY7QDVMNScaup8X-R4x9ZwIPaGc3BtXkg130_assertion
dcterms:description
"[Long term treatment with IFN2b is able to induce 'minimal residual disease' with very low JAK2 V617F allele burden and may induce profound, and in some patients total, regression of histomorphological bone marrow features of PV.]. 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:19941739
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP519521.RA2HREzbnCPQMY7QDVMNScaup8X-R4x9ZwIPaGc3BtXkg130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:42:47+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}