@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP978560.RAAWKh17PWoruPl9XBU1dwti6GmbsXjwiJl5-QC9ZLkY8
> .
@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/v3.0.0/void/
> .
dgn-np:NP978560.RAAWKh17PWoruPl9XBU1dwti6GmbsXjwiJl5-QC9ZLkY8130_head
{
this:
np:hasAssertion
dgn-np:NP978560.RAAWKh17PWoruPl9XBU1dwti6GmbsXjwiJl5-QC9ZLkY8130_assertion
;
np:hasProvenance
dgn-np:NP978560.RAAWKh17PWoruPl9XBU1dwti6GmbsXjwiJl5-QC9ZLkY8130_provenance
;
np:hasPublicationInfo
dgn-np:NP978560.RAAWKh17PWoruPl9XBU1dwti6GmbsXjwiJl5-QC9ZLkY8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP978560.RAAWKh17PWoruPl9XBU1dwti6GmbsXjwiJl5-QC9ZLkY8130_assertion
a
np:Assertion
.
dgn-np:NP978560.RAAWKh17PWoruPl9XBU1dwti6GmbsXjwiJl5-QC9ZLkY8130_provenance
a
np:Provenance
.
dgn-np:NP978560.RAAWKh17PWoruPl9XBU1dwti6GmbsXjwiJl5-QC9ZLkY8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP978560.RAAWKh17PWoruPl9XBU1dwti6GmbsXjwiJl5-QC9ZLkY8130_assertion
{
miriam-gene:171023
a
ncit:C16612
.
lld:C0032463
a
ncit:C7057
.
dgn-gda:DGN849dd37fd187deeb3b7d515dd15658bb
sio:SIO_000628
miriam-gene:171023
,
lld:C0032463
;
a
sio:SIO_001122
.
}
dgn-np:NP978560.RAAWKh17PWoruPl9XBU1dwti6GmbsXjwiJl5-QC9ZLkY8130_provenance
{
dgn-np:NP978560.RAAWKh17PWoruPl9XBU1dwti6GmbsXjwiJl5-QC9ZLkY8130_assertion
dcterms:description
"[We have studied the mutational status of TET2 (complete coding region), ASXL1 (exon12), IDH1 (R132), IDH2 (R140 and R172), and c-CBL (exons 8 and 9) in 62 MPN patients (52 essential thrombocythemia (ET), five polycythemia vera (PV), and five primary myelofibrosis (PMF)) negative for both JAK2 (V617F and exon 12) and MPL (exon 10) mutations.]. 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:21904853
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP978560.RAAWKh17PWoruPl9XBU1dwti6GmbsXjwiJl5-QC9ZLkY8130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:37+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}