@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP761131.RA8rO0KKJRbZsLG7rS2EJ2ZNdcSphQaifaR-QWVTNppuA
> .
@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:NP761131.RA8rO0KKJRbZsLG7rS2EJ2ZNdcSphQaifaR-QWVTNppuA130_head
{
this:
np:hasAssertion
dgn-np:NP761131.RA8rO0KKJRbZsLG7rS2EJ2ZNdcSphQaifaR-QWVTNppuA130_assertion
;
np:hasProvenance
dgn-np:NP761131.RA8rO0KKJRbZsLG7rS2EJ2ZNdcSphQaifaR-QWVTNppuA130_provenance
;
np:hasPublicationInfo
dgn-np:NP761131.RA8rO0KKJRbZsLG7rS2EJ2ZNdcSphQaifaR-QWVTNppuA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP761131.RA8rO0KKJRbZsLG7rS2EJ2ZNdcSphQaifaR-QWVTNppuA130_assertion
a
np:Assertion
.
dgn-np:NP761131.RA8rO0KKJRbZsLG7rS2EJ2ZNdcSphQaifaR-QWVTNppuA130_provenance
a
np:Provenance
.
dgn-np:NP761131.RA8rO0KKJRbZsLG7rS2EJ2ZNdcSphQaifaR-QWVTNppuA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP761131.RA8rO0KKJRbZsLG7rS2EJ2ZNdcSphQaifaR-QWVTNppuA130_assertion
{
miriam-gene:3717
a
ncit:C16612
.
lld:C0023480
a
ncit:C7057
.
dgn-gda:DGNdd6dbe99b150f7f39e54882f4b79a68f
sio:SIO_000628
miriam-gene:3717
,
lld:C0023480
;
a
sio:SIO_001121
.
}
dgn-np:NP761131.RA8rO0KKJRbZsLG7rS2EJ2ZNdcSphQaifaR-QWVTNppuA130_provenance
{
dgn-np:NP761131.RA8rO0KKJRbZsLG7rS2EJ2ZNdcSphQaifaR-QWVTNppuA130_assertion
dcterms:description
"[A recurrent somatic activating mutation in the nonreceptor tyrosine kinase JAK2 (JAK2V617F) occurs in the majority of patients with the myeloproliferative disorders polycythemia vera, essential thrombocythemia, myelofibrosis with myeloid metaplasia, and, less commonly, chronic myelomonocytic leukemia.]. 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:16365288
;
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:NP761131.RA8rO0KKJRbZsLG7rS2EJ2ZNdcSphQaifaR-QWVTNppuA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:40+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" .
}