@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP559465.RA2qkAEMecmVo_W5PoxmehQUU9V1m7z6EtYd1EJ1_h6kE
> .
@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:NP559465.RA2qkAEMecmVo_W5PoxmehQUU9V1m7z6EtYd1EJ1_h6kE130_head
{
this:
np:hasAssertion
dgn-np:NP559465.RA2qkAEMecmVo_W5PoxmehQUU9V1m7z6EtYd1EJ1_h6kE130_assertion
;
np:hasProvenance
dgn-np:NP559465.RA2qkAEMecmVo_W5PoxmehQUU9V1m7z6EtYd1EJ1_h6kE130_provenance
;
np:hasPublicationInfo
dgn-np:NP559465.RA2qkAEMecmVo_W5PoxmehQUU9V1m7z6EtYd1EJ1_h6kE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP559465.RA2qkAEMecmVo_W5PoxmehQUU9V1m7z6EtYd1EJ1_h6kE130_assertion
a
np:Assertion
.
dgn-np:NP559465.RA2qkAEMecmVo_W5PoxmehQUU9V1m7z6EtYd1EJ1_h6kE130_provenance
a
np:Provenance
.
dgn-np:NP559465.RA2qkAEMecmVo_W5PoxmehQUU9V1m7z6EtYd1EJ1_h6kE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP559465.RA2qkAEMecmVo_W5PoxmehQUU9V1m7z6EtYd1EJ1_h6kE130_assertion
{
miriam-gene:2056
a
ncit:C16612
.
lld:C0014800
a
ncit:C7057
.
dgn-gda:DGN9b501d232fed89771c0ffc63aeb504c3
sio:SIO_000628
miriam-gene:2056
,
lld:C0014800
;
a
sio:SIO_001121
.
}
dgn-np:NP559465.RA2qkAEMecmVo_W5PoxmehQUU9V1m7z6EtYd1EJ1_h6kE130_provenance
{
dgn-np:NP559465.RA2qkAEMecmVo_W5PoxmehQUU9V1m7z6EtYd1EJ1_h6kE130_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-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:NP559465.RA2qkAEMecmVo_W5PoxmehQUU9V1m7z6EtYd1EJ1_h6kE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:37+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" .
}