@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP851289.RACku84r_1gwJAeITKt1wY3_oRJa5Br2ZzciK9FoU8TkU
> .
@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:NP851289.RACku84r_1gwJAeITKt1wY3_oRJa5Br2ZzciK9FoU8TkU130_head
{
this:
np:hasAssertion
dgn-np:NP851289.RACku84r_1gwJAeITKt1wY3_oRJa5Br2ZzciK9FoU8TkU130_assertion
;
np:hasProvenance
dgn-np:NP851289.RACku84r_1gwJAeITKt1wY3_oRJa5Br2ZzciK9FoU8TkU130_provenance
;
np:hasPublicationInfo
dgn-np:NP851289.RACku84r_1gwJAeITKt1wY3_oRJa5Br2ZzciK9FoU8TkU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP851289.RACku84r_1gwJAeITKt1wY3_oRJa5Br2ZzciK9FoU8TkU130_assertion
a
np:Assertion
.
dgn-np:NP851289.RACku84r_1gwJAeITKt1wY3_oRJa5Br2ZzciK9FoU8TkU130_provenance
a
np:Provenance
.
dgn-np:NP851289.RACku84r_1gwJAeITKt1wY3_oRJa5Br2ZzciK9FoU8TkU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP851289.RACku84r_1gwJAeITKt1wY3_oRJa5Br2ZzciK9FoU8TkU130_assertion
{
miriam-gene:4352
a
ncit:C16612
.
lld:C0008626
a
ncit:C7057
.
dgn-gda:DGN37f4a5459366d1884f84dd91338573fc
sio:SIO_000628
miriam-gene:4352
,
lld:C0008626
;
a
sio:SIO_001121
.
}
dgn-np:NP851289.RACku84r_1gwJAeITKt1wY3_oRJa5Br2ZzciK9FoU8TkU130_provenance
{
dgn-np:NP851289.RACku84r_1gwJAeITKt1wY3_oRJa5Br2ZzciK9FoU8TkU130_assertion
dcterms:description
"[After the discovery of JAK and MPL mutations, continual technological advances have led to the identification of increasing numbers of genetic defects in MPN patients, most of them chromosomal aberrations such as deletions and acquired uniparental disomies.]. 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:21062246
;
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:NP851289.RACku84r_1gwJAeITKt1wY3_oRJa5Br2ZzciK9FoU8TkU130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:10+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" .
}