@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP71497.RA4o9iYGYNtd1XIxpICGkzYVnrYNIPsDAbYU2vZ8L457c
> .
@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:NP71497.RA4o9iYGYNtd1XIxpICGkzYVnrYNIPsDAbYU2vZ8L457c130_head
{
this:
np:hasAssertion
dgn-np:NP71497.RA4o9iYGYNtd1XIxpICGkzYVnrYNIPsDAbYU2vZ8L457c130_assertion
;
np:hasProvenance
dgn-np:NP71497.RA4o9iYGYNtd1XIxpICGkzYVnrYNIPsDAbYU2vZ8L457c130_provenance
;
np:hasPublicationInfo
dgn-np:NP71497.RA4o9iYGYNtd1XIxpICGkzYVnrYNIPsDAbYU2vZ8L457c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP71497.RA4o9iYGYNtd1XIxpICGkzYVnrYNIPsDAbYU2vZ8L457c130_assertion
a
np:Assertion
.
dgn-np:NP71497.RA4o9iYGYNtd1XIxpICGkzYVnrYNIPsDAbYU2vZ8L457c130_provenance
a
np:Provenance
.
dgn-np:NP71497.RA4o9iYGYNtd1XIxpICGkzYVnrYNIPsDAbYU2vZ8L457c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP71497.RA4o9iYGYNtd1XIxpICGkzYVnrYNIPsDAbYU2vZ8L457c130_assertion
{
miriam-gene:3717
a
ncit:C16612
.
lld:C0027022
a
ncit:C7057
.
dgn-gda:DGN051f1e423c629ed003edff1ee9b0e721
sio:SIO_000628
miriam-gene:3717
,
lld:C0027022
;
a
sio:SIO_001122
.
}
dgn-np:NP71497.RA4o9iYGYNtd1XIxpICGkzYVnrYNIPsDAbYU2vZ8L457c130_provenance
{
dgn-np:NP71497.RA4o9iYGYNtd1XIxpICGkzYVnrYNIPsDAbYU2vZ8L457c130_assertion
dcterms:description
"[Since variability in the JAK2(V617F) allele burden is partly responsible for the distinct phenotypes seen in the myeloproliferative disorders, the objective of this study was to identify modifiers of the allele burden.]. 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:20133898
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP71497.RA4o9iYGYNtd1XIxpICGkzYVnrYNIPsDAbYU2vZ8L457c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:34+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" .
}