@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP641451.RAf6SF8jyXA7N9poC8gMWKZHahYHn0wrVX8zhBsqGl4Is
> .
@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:NP641451.RAf6SF8jyXA7N9poC8gMWKZHahYHn0wrVX8zhBsqGl4Is130_head
{
this:
np:hasAssertion
dgn-np:NP641451.RAf6SF8jyXA7N9poC8gMWKZHahYHn0wrVX8zhBsqGl4Is130_assertion
;
np:hasProvenance
dgn-np:NP641451.RAf6SF8jyXA7N9poC8gMWKZHahYHn0wrVX8zhBsqGl4Is130_provenance
;
np:hasPublicationInfo
dgn-np:NP641451.RAf6SF8jyXA7N9poC8gMWKZHahYHn0wrVX8zhBsqGl4Is130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP641451.RAf6SF8jyXA7N9poC8gMWKZHahYHn0wrVX8zhBsqGl4Is130_assertion
a
np:Assertion
.
dgn-np:NP641451.RAf6SF8jyXA7N9poC8gMWKZHahYHn0wrVX8zhBsqGl4Is130_provenance
a
np:Provenance
.
dgn-np:NP641451.RAf6SF8jyXA7N9poC8gMWKZHahYHn0wrVX8zhBsqGl4Is130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP641451.RAf6SF8jyXA7N9poC8gMWKZHahYHn0wrVX8zhBsqGl4Is130_assertion
{
miriam-gene:3717
a
ncit:C16612
.
lld:C0024305
a
ncit:C7057
.
dgn-gda:DGNab713066f705c89193c194fa0b42d7b3
sio:SIO_000628
miriam-gene:3717
,
lld:C0024305
;
a
sio:SIO_001121
.
}
dgn-np:NP641451.RAf6SF8jyXA7N9poC8gMWKZHahYHn0wrVX8zhBsqGl4Is130_provenance
{
dgn-np:NP641451.RAf6SF8jyXA7N9poC8gMWKZHahYHn0wrVX8zhBsqGl4Is130_assertion
dcterms:description
"[This case may be of interest not only due to the rare coexistence of PMN and NHL, but also because of the undetermined clinical significance of JAK2 mutation in this 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:21508404
;
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:NP641451.RAf6SF8jyXA7N9poC8gMWKZHahYHn0wrVX8zhBsqGl4Is130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:26+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" .
}