@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP360406.RASTw2sjQVnx3IDq7oUzT13tTkiguIq2t1_kCnihnvzCU
> .
@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:NP360406.RASTw2sjQVnx3IDq7oUzT13tTkiguIq2t1_kCnihnvzCU130_head
{
this:
np:hasAssertion
dgn-np:NP360406.RASTw2sjQVnx3IDq7oUzT13tTkiguIq2t1_kCnihnvzCU130_assertion
;
np:hasProvenance
dgn-np:NP360406.RASTw2sjQVnx3IDq7oUzT13tTkiguIq2t1_kCnihnvzCU130_provenance
;
np:hasPublicationInfo
dgn-np:NP360406.RASTw2sjQVnx3IDq7oUzT13tTkiguIq2t1_kCnihnvzCU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP360406.RASTw2sjQVnx3IDq7oUzT13tTkiguIq2t1_kCnihnvzCU130_assertion
a
np:Assertion
.
dgn-np:NP360406.RASTw2sjQVnx3IDq7oUzT13tTkiguIq2t1_kCnihnvzCU130_provenance
a
np:Provenance
.
dgn-np:NP360406.RASTw2sjQVnx3IDq7oUzT13tTkiguIq2t1_kCnihnvzCU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP360406.RASTw2sjQVnx3IDq7oUzT13tTkiguIq2t1_kCnihnvzCU130_assertion
{
miriam-gene:25
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGN95cc200de14ec364404e850887205c01
sio:SIO_000628
miriam-gene:25
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP360406.RASTw2sjQVnx3IDq7oUzT13tTkiguIq2t1_kCnihnvzCU130_provenance
{
dgn-np:NP360406.RASTw2sjQVnx3IDq7oUzT13tTkiguIq2t1_kCnihnvzCU130_assertion
dcterms:description
"[BCR-ABL-negative myeloproliferative neoplasms (MPNs) are most frequently characterized by the JAK2V617F gain-of-function mutation, but several studies showed that JAK2V617F may not be the initiating event in MPN development, and recent publications indicate that additional alterations such as chromatin modification and microRNA (miRNA) deregulation may have an important role in MPN pathogenesis.]. 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:22864358
;
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:NP360406.RASTw2sjQVnx3IDq7oUzT13tTkiguIq2t1_kCnihnvzCU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:31+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" .
}