@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP501378.RAO-f6KIokurzQ4FRl59lWc4x5nk_gV4r2sSDNLXT83bk
> .
@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:NP501378.RAO-f6KIokurzQ4FRl59lWc4x5nk_gV4r2sSDNLXT83bk130_head
{
this:
np:hasAssertion
dgn-np:NP501378.RAO-f6KIokurzQ4FRl59lWc4x5nk_gV4r2sSDNLXT83bk130_assertion
;
np:hasProvenance
dgn-np:NP501378.RAO-f6KIokurzQ4FRl59lWc4x5nk_gV4r2sSDNLXT83bk130_provenance
;
np:hasPublicationInfo
dgn-np:NP501378.RAO-f6KIokurzQ4FRl59lWc4x5nk_gV4r2sSDNLXT83bk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP501378.RAO-f6KIokurzQ4FRl59lWc4x5nk_gV4r2sSDNLXT83bk130_assertion
a
np:Assertion
.
dgn-np:NP501378.RAO-f6KIokurzQ4FRl59lWc4x5nk_gV4r2sSDNLXT83bk130_provenance
a
np:Provenance
.
dgn-np:NP501378.RAO-f6KIokurzQ4FRl59lWc4x5nk_gV4r2sSDNLXT83bk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP501378.RAO-f6KIokurzQ4FRl59lWc4x5nk_gV4r2sSDNLXT83bk130_assertion
{
miriam-gene:83886
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGNfb4239756bd2810167d42302a1c2f43f
sio:SIO_000628
miriam-gene:83886
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP501378.RAO-f6KIokurzQ4FRl59lWc4x5nk_gV4r2sSDNLXT83bk130_provenance
{
dgn-np:NP501378.RAO-f6KIokurzQ4FRl59lWc4x5nk_gV4r2sSDNLXT83bk130_assertion
dcterms:description
"[The discovery of JAK2 and MPL mutations in patients with myeloproliferative neoplasms (MPNs) provided important insight into the genetic basis of these disorders and led to the development of JAK2 kinase inhibitors for MPN therapy.]. 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:20154217
;
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:NP501378.RAO-f6KIokurzQ4FRl59lWc4x5nk_gV4r2sSDNLXT83bk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:59+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" .
}