@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP465636.RAwIp87dfmgwJ-eXVEaJje6wkexZEGLaLWHh-30zEyxOY
> .
@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:NP465636.RAwIp87dfmgwJ-eXVEaJje6wkexZEGLaLWHh-30zEyxOY130_head
{
this:
np:hasAssertion
dgn-np:NP465636.RAwIp87dfmgwJ-eXVEaJje6wkexZEGLaLWHh-30zEyxOY130_assertion
;
np:hasProvenance
dgn-np:NP465636.RAwIp87dfmgwJ-eXVEaJje6wkexZEGLaLWHh-30zEyxOY130_provenance
;
np:hasPublicationInfo
dgn-np:NP465636.RAwIp87dfmgwJ-eXVEaJje6wkexZEGLaLWHh-30zEyxOY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP465636.RAwIp87dfmgwJ-eXVEaJje6wkexZEGLaLWHh-30zEyxOY130_assertion
a
np:Assertion
.
dgn-np:NP465636.RAwIp87dfmgwJ-eXVEaJje6wkexZEGLaLWHh-30zEyxOY130_provenance
a
np:Provenance
.
dgn-np:NP465636.RAwIp87dfmgwJ-eXVEaJje6wkexZEGLaLWHh-30zEyxOY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP465636.RAwIp87dfmgwJ-eXVEaJje6wkexZEGLaLWHh-30zEyxOY130_assertion
{
miriam-gene:3815
a
ncit:C16612
.
lld:C3463824
a
ncit:C7057
.
dgn-gda:DGN574309b121735f45ba4153eeb29a277e
sio:SIO_000628
miriam-gene:3815
,
lld:C3463824
;
a
sio:SIO_001121
.
}
dgn-np:NP465636.RAwIp87dfmgwJ-eXVEaJje6wkexZEGLaLWHh-30zEyxOY130_provenance
{
dgn-np:NP465636.RAwIp87dfmgwJ-eXVEaJje6wkexZEGLaLWHh-30zEyxOY130_assertion
dcterms:description
"[These observations suggest that KIT gene mutations identified in the advanced stage of MDS, and genetic abnormality in the KIT gene, particularly at codon 816, might be additional events that contribute to the progression of MDS to AML.]. 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:16533529
;
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:NP465636.RAwIp87dfmgwJ-eXVEaJje6wkexZEGLaLWHh-30zEyxOY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:39+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" .
}