@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP657089.RARHlt_DgO3nXMfDvIjU2z6jQdkqwghldmO3pLXpVnWHs
> .
@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:NP657089.RARHlt_DgO3nXMfDvIjU2z6jQdkqwghldmO3pLXpVnWHs130_head
{
this:
np:hasAssertion
dgn-np:NP657089.RARHlt_DgO3nXMfDvIjU2z6jQdkqwghldmO3pLXpVnWHs130_assertion
;
np:hasProvenance
dgn-np:NP657089.RARHlt_DgO3nXMfDvIjU2z6jQdkqwghldmO3pLXpVnWHs130_provenance
;
np:hasPublicationInfo
dgn-np:NP657089.RARHlt_DgO3nXMfDvIjU2z6jQdkqwghldmO3pLXpVnWHs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP657089.RARHlt_DgO3nXMfDvIjU2z6jQdkqwghldmO3pLXpVnWHs130_assertion
a
np:Assertion
.
dgn-np:NP657089.RARHlt_DgO3nXMfDvIjU2z6jQdkqwghldmO3pLXpVnWHs130_provenance
a
np:Provenance
.
dgn-np:NP657089.RARHlt_DgO3nXMfDvIjU2z6jQdkqwghldmO3pLXpVnWHs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP657089.RARHlt_DgO3nXMfDvIjU2z6jQdkqwghldmO3pLXpVnWHs130_assertion
{
miriam-gene:3717
a
ncit:C16612
.
lld:C0027013
a
ncit:C7057
.
dgn-gda:DGN4a841c4c588835b0a2182b1f97867a60
sio:SIO_000628
miriam-gene:3717
,
lld:C0027013
;
a
sio:SIO_001121
.
}
dgn-np:NP657089.RARHlt_DgO3nXMfDvIjU2z6jQdkqwghldmO3pLXpVnWHs130_provenance
{
dgn-np:NP657089.RARHlt_DgO3nXMfDvIjU2z6jQdkqwghldmO3pLXpVnWHs130_assertion
dcterms:description
"[In the current study, mutation analysis for JAK2(V617F) was performed in peripheral blood mononuclear cells (PBMC) from 157 patients with myelofibrosis with myeloid metaplasia (MMM) including 117 with agnogenic (AMM), 22 with postpolycythaemic (PPMM), and 18 with post-thrombocythaemic (PTMM) myeloid metaplasia.]. 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:16225651
;
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:NP657089.RARHlt_DgO3nXMfDvIjU2z6jQdkqwghldmO3pLXpVnWHs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:35+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" .
}