@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP20667.RAlhaewSH3MXvydIC6AGc6yzzcPSmMnpBQQcf5ACXZqVo
> .
@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:NP20667.RAlhaewSH3MXvydIC6AGc6yzzcPSmMnpBQQcf5ACXZqVo130_head
{
this:
np:hasAssertion
dgn-np:NP20667.RAlhaewSH3MXvydIC6AGc6yzzcPSmMnpBQQcf5ACXZqVo130_assertion
;
np:hasProvenance
dgn-np:NP20667.RAlhaewSH3MXvydIC6AGc6yzzcPSmMnpBQQcf5ACXZqVo130_provenance
;
np:hasPublicationInfo
dgn-np:NP20667.RAlhaewSH3MXvydIC6AGc6yzzcPSmMnpBQQcf5ACXZqVo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP20667.RAlhaewSH3MXvydIC6AGc6yzzcPSmMnpBQQcf5ACXZqVo130_assertion
a
np:Assertion
.
dgn-np:NP20667.RAlhaewSH3MXvydIC6AGc6yzzcPSmMnpBQQcf5ACXZqVo130_provenance
a
np:Provenance
.
dgn-np:NP20667.RAlhaewSH3MXvydIC6AGc6yzzcPSmMnpBQQcf5ACXZqVo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP20667.RAlhaewSH3MXvydIC6AGc6yzzcPSmMnpBQQcf5ACXZqVo130_assertion
{
miriam-gene:3717
a
ncit:C16612
.
lld:C0040028
a
ncit:C7057
.
dgn-gda:DGNb17531b523bee0b79de1b3c97a77a4e3
sio:SIO_000628
miriam-gene:3717
,
lld:C0040028
;
a
sio:SIO_001121
.
}
dgn-np:NP20667.RAlhaewSH3MXvydIC6AGc6yzzcPSmMnpBQQcf5ACXZqVo130_provenance
{
dgn-np:NP20667.RAlhaewSH3MXvydIC6AGc6yzzcPSmMnpBQQcf5ACXZqVo130_assertion
dcterms:description
"[The frequency of V617F was 65 percent among patients with polycythemia vera (83 of 128), 57 percent among patients with idiopathic myelofibrosis (13 of 23), and 23 percent among patients with essential thrombocythemia (21 of 93).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:15858187
;
prov:wasDerivedFrom
dgn-void:ctd_human-20130708
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20130708
pav:importedOn
"2013-07-24"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP20667.RAlhaewSH3MXvydIC6AGc6yzzcPSmMnpBQQcf5ACXZqVo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:08+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" .
}