@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP377827.RA4XcWigBDavshhiL916Mgv8Ew2cK0lyRIbC1CCE1R1yU
> .
@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:NP377827.RA4XcWigBDavshhiL916Mgv8Ew2cK0lyRIbC1CCE1R1yU130_head
{
this:
np:hasAssertion
dgn-np:NP377827.RA4XcWigBDavshhiL916Mgv8Ew2cK0lyRIbC1CCE1R1yU130_assertion
;
np:hasProvenance
dgn-np:NP377827.RA4XcWigBDavshhiL916Mgv8Ew2cK0lyRIbC1CCE1R1yU130_provenance
;
np:hasPublicationInfo
dgn-np:NP377827.RA4XcWigBDavshhiL916Mgv8Ew2cK0lyRIbC1CCE1R1yU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP377827.RA4XcWigBDavshhiL916Mgv8Ew2cK0lyRIbC1CCE1R1yU130_assertion
a
np:Assertion
.
dgn-np:NP377827.RA4XcWigBDavshhiL916Mgv8Ew2cK0lyRIbC1CCE1R1yU130_provenance
a
np:Provenance
.
dgn-np:NP377827.RA4XcWigBDavshhiL916Mgv8Ew2cK0lyRIbC1CCE1R1yU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP377827.RA4XcWigBDavshhiL916Mgv8Ew2cK0lyRIbC1CCE1R1yU130_assertion
{
miriam-gene:2056
a
ncit:C16612
.
lld:C0014800
a
ncit:C7057
.
dgn-gda:DGN2000e6b58145e6293cd3e6ac8a0e528d
sio:SIO_000628
miriam-gene:2056
,
lld:C0014800
;
a
sio:SIO_001122
.
}
dgn-np:NP377827.RA4XcWigBDavshhiL916Mgv8Ew2cK0lyRIbC1CCE1R1yU130_provenance
{
dgn-np:NP377827.RA4XcWigBDavshhiL916Mgv8Ew2cK0lyRIbC1CCE1R1yU130_assertion
dcterms:description
"[Clinically suspected PV with low serum erythropoietin and absent JAK2(V617F), together with the bone marrow findings of erythroid hyperplasia and subtle megakaryocytic atypia, should prompt an evaluation for an exon 12 mutation.]. 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:20472853
;
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:NP377827.RA4XcWigBDavshhiL916Mgv8Ew2cK0lyRIbC1CCE1R1yU130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:18+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" .
}