@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP555067.RAqFwuK0sNiJOqqRAaC12U0iqO1Hc-0ay2qsvApK9QMFk
> .
@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:NP555067.RAqFwuK0sNiJOqqRAaC12U0iqO1Hc-0ay2qsvApK9QMFk130_head
{
this:
np:hasAssertion
dgn-np:NP555067.RAqFwuK0sNiJOqqRAaC12U0iqO1Hc-0ay2qsvApK9QMFk130_assertion
;
np:hasProvenance
dgn-np:NP555067.RAqFwuK0sNiJOqqRAaC12U0iqO1Hc-0ay2qsvApK9QMFk130_provenance
;
np:hasPublicationInfo
dgn-np:NP555067.RAqFwuK0sNiJOqqRAaC12U0iqO1Hc-0ay2qsvApK9QMFk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP555067.RAqFwuK0sNiJOqqRAaC12U0iqO1Hc-0ay2qsvApK9QMFk130_assertion
a
np:Assertion
.
dgn-np:NP555067.RAqFwuK0sNiJOqqRAaC12U0iqO1Hc-0ay2qsvApK9QMFk130_provenance
a
np:Provenance
.
dgn-np:NP555067.RAqFwuK0sNiJOqqRAaC12U0iqO1Hc-0ay2qsvApK9QMFk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP555067.RAqFwuK0sNiJOqqRAaC12U0iqO1Hc-0ay2qsvApK9QMFk130_assertion
{
miriam-gene:83886
a
ncit:C16612
.
lld:C1292778
a
ncit:C7057
.
dgn-gda:DGN6dac3453cc552a07d19dd0cf14550767
sio:SIO_000628
miriam-gene:83886
,
lld:C1292778
;
a
sio:SIO_001121
.
}
dgn-np:NP555067.RAqFwuK0sNiJOqqRAaC12U0iqO1Hc-0ay2qsvApK9QMFk130_provenance
{
dgn-np:NP555067.RAqFwuK0sNiJOqqRAaC12U0iqO1Hc-0ay2qsvApK9QMFk130_assertion
dcterms:description
"[Our findings argue that the mutational order of events in MPN and sAML varies in different patients, and that TET2 and ASXL1 mutations have distinct roles in MPN pathogenesis and leukemic transformation.]. 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:20068184
;
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:NP555067.RAqFwuK0sNiJOqqRAaC12U0iqO1Hc-0ay2qsvApK9QMFk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:34+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" .
}