@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP189477.RA3yKRXbn3G8pqvMG4Ga7Qjad8Sm2BFx3EXL8FadyfYd4
> .
@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:NP189477.RA3yKRXbn3G8pqvMG4Ga7Qjad8Sm2BFx3EXL8FadyfYd4130_head
{
this:
np:hasAssertion
dgn-np:NP189477.RA3yKRXbn3G8pqvMG4Ga7Qjad8Sm2BFx3EXL8FadyfYd4130_assertion
;
np:hasProvenance
dgn-np:NP189477.RA3yKRXbn3G8pqvMG4Ga7Qjad8Sm2BFx3EXL8FadyfYd4130_provenance
;
np:hasPublicationInfo
dgn-np:NP189477.RA3yKRXbn3G8pqvMG4Ga7Qjad8Sm2BFx3EXL8FadyfYd4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP189477.RA3yKRXbn3G8pqvMG4Ga7Qjad8Sm2BFx3EXL8FadyfYd4130_assertion
a
np:Assertion
.
dgn-np:NP189477.RA3yKRXbn3G8pqvMG4Ga7Qjad8Sm2BFx3EXL8FadyfYd4130_provenance
a
np:Provenance
.
dgn-np:NP189477.RA3yKRXbn3G8pqvMG4Ga7Qjad8Sm2BFx3EXL8FadyfYd4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP189477.RA3yKRXbn3G8pqvMG4Ga7Qjad8Sm2BFx3EXL8FadyfYd4130_assertion
{
miriam-gene:2523
a
ncit:C16612
.
lld:C0032463
a
ncit:C7057
.
dgn-gda:DGNc65e3de7088f47b10319afd5119bc8b4
sio:SIO_000628
miriam-gene:2523
,
lld:C0032463
;
a
sio:SIO_001121
.
}
dgn-np:NP189477.RA3yKRXbn3G8pqvMG4Ga7Qjad8Sm2BFx3EXL8FadyfYd4130_provenance
{
dgn-np:NP189477.RA3yKRXbn3G8pqvMG4Ga7Qjad8Sm2BFx3EXL8FadyfYd4130_assertion
dcterms:description
"[Here we isolated and characterized hematopoietic stem cells (HSC) and myeloid progenitors from 16 PV patient samples and 14 normal individuals, testing whether the JAK2 mutation could be found at the level of stem or progenitor cells and whether the JAK2 V617F-positive cells had altered differentiation potential.]. 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:16603627
;
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:NP189477.RA3yKRXbn3G8pqvMG4Ga7Qjad8Sm2BFx3EXL8FadyfYd4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:44+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" .
}