@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP567261.RAQHDkrJjpZBnJOB2Ad8s31Drqv3dWoXBT0FQXJkZgO_0
> .
@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:NP567261.RAQHDkrJjpZBnJOB2Ad8s31Drqv3dWoXBT0FQXJkZgO_0130_head
{
this:
np:hasAssertion
dgn-np:NP567261.RAQHDkrJjpZBnJOB2Ad8s31Drqv3dWoXBT0FQXJkZgO_0130_assertion
;
np:hasProvenance
dgn-np:NP567261.RAQHDkrJjpZBnJOB2Ad8s31Drqv3dWoXBT0FQXJkZgO_0130_provenance
;
np:hasPublicationInfo
dgn-np:NP567261.RAQHDkrJjpZBnJOB2Ad8s31Drqv3dWoXBT0FQXJkZgO_0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP567261.RAQHDkrJjpZBnJOB2Ad8s31Drqv3dWoXBT0FQXJkZgO_0130_assertion
a
np:Assertion
.
dgn-np:NP567261.RAQHDkrJjpZBnJOB2Ad8s31Drqv3dWoXBT0FQXJkZgO_0130_provenance
a
np:Provenance
.
dgn-np:NP567261.RAQHDkrJjpZBnJOB2Ad8s31Drqv3dWoXBT0FQXJkZgO_0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP567261.RAQHDkrJjpZBnJOB2Ad8s31Drqv3dWoXBT0FQXJkZgO_0130_assertion
{
miriam-gene:4352
a
ncit:C16612
.
lld:C0026987
a
ncit:C7057
.
dgn-gda:DGN69e5922d368c80c27b0289449a98adae
sio:SIO_000628
miriam-gene:4352
,
lld:C0026987
;
a
sio:SIO_001122
.
}
dgn-np:NP567261.RAQHDkrJjpZBnJOB2Ad8s31Drqv3dWoXBT0FQXJkZgO_0130_provenance
{
dgn-np:NP567261.RAQHDkrJjpZBnJOB2Ad8s31Drqv3dWoXBT0FQXJkZgO_0130_assertion
dcterms:description
"[Given their diagnostic relevance, it is also beneficial and relatively straightforward to screen JAK2 V617F negative patients for JAK2 exon 12 mutations (in the case of erythrocytosis) or MPL exon 10 mutations (thrombocytosis or myelofibrosis) using appropriate assays.]. 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:23057517
;
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:NP567261.RAQHDkrJjpZBnJOB2Ad8s31Drqv3dWoXBT0FQXJkZgO_0130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:17+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" .
}