@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP563703.RAehfk90j0XN4aU6Imtq6-mfZ8GjkWD9nN8wClpGX4D5g
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP563703.RAehfk90j0XN4aU6Imtq6-mfZ8GjkWD9nN8wClpGX4D5g130_head
{
this:
np:hasAssertion
dgn-np:NP563703.RAehfk90j0XN4aU6Imtq6-mfZ8GjkWD9nN8wClpGX4D5g130_assertion
;
np:hasProvenance
dgn-np:NP563703.RAehfk90j0XN4aU6Imtq6-mfZ8GjkWD9nN8wClpGX4D5g130_provenance
;
np:hasPublicationInfo
dgn-np:NP563703.RAehfk90j0XN4aU6Imtq6-mfZ8GjkWD9nN8wClpGX4D5g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP563703.RAehfk90j0XN4aU6Imtq6-mfZ8GjkWD9nN8wClpGX4D5g130_assertion
a
np:Assertion
.
dgn-np:NP563703.RAehfk90j0XN4aU6Imtq6-mfZ8GjkWD9nN8wClpGX4D5g130_provenance
a
np:Provenance
.
dgn-np:NP563703.RAehfk90j0XN4aU6Imtq6-mfZ8GjkWD9nN8wClpGX4D5g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP563703.RAehfk90j0XN4aU6Imtq6-mfZ8GjkWD9nN8wClpGX4D5g130_assertion
{
miriam-gene:3717
a
ncit:C16612
.
lld:C0026987
a
ncit:C7057
.
dgn-gda:DGNc125252f960315174de6b0db1833d820
sio:SIO_000628
miriam-gene:3717
,
lld:C0026987
;
a
sio:SIO_001121
.
}
dgn-np:NP563703.RAehfk90j0XN4aU6Imtq6-mfZ8GjkWD9nN8wClpGX4D5g130_provenance
{
dgn-np:NP563703.RAehfk90j0XN4aU6Imtq6-mfZ8GjkWD9nN8wClpGX4D5g130_assertion
dcterms:description
"[Comparisons of JAK2 mutational status to clonality of hematopoiesis in essential thrombocythemia on the one hand, and to activation of transcription factors in myelofibrosis with myeloid metaplasia on the other hand, suggest that JAK2 mutation could be a second genetic event in a subset of patients.]. 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:16901656
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP563703.RAehfk90j0XN4aU6Imtq6-mfZ8GjkWD9nN8wClpGX4D5g130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:00+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}