@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP440249.RAcBDz1_lgtSnEj-p5JadAJ8002Unu2MAZlvq_J9UWEe4
> .
@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:NP440249.RAcBDz1_lgtSnEj-p5JadAJ8002Unu2MAZlvq_J9UWEe4130_head
{
this:
np:hasAssertion
dgn-np:NP440249.RAcBDz1_lgtSnEj-p5JadAJ8002Unu2MAZlvq_J9UWEe4130_assertion
;
np:hasProvenance
dgn-np:NP440249.RAcBDz1_lgtSnEj-p5JadAJ8002Unu2MAZlvq_J9UWEe4130_provenance
;
np:hasPublicationInfo
dgn-np:NP440249.RAcBDz1_lgtSnEj-p5JadAJ8002Unu2MAZlvq_J9UWEe4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP440249.RAcBDz1_lgtSnEj-p5JadAJ8002Unu2MAZlvq_J9UWEe4130_assertion
a
np:Assertion
.
dgn-np:NP440249.RAcBDz1_lgtSnEj-p5JadAJ8002Unu2MAZlvq_J9UWEe4130_provenance
a
np:Provenance
.
dgn-np:NP440249.RAcBDz1_lgtSnEj-p5JadAJ8002Unu2MAZlvq_J9UWEe4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP440249.RAcBDz1_lgtSnEj-p5JadAJ8002Unu2MAZlvq_J9UWEe4130_assertion
{
miriam-gene:3717
a
ncit:C16612
.
lld:C2939461
a
ncit:C7057
.
dgn-gda:DGN706b1d30a4089bb84f3f4f50ad1fac99
sio:SIO_000628
miriam-gene:3717
,
lld:C2939461
;
a
sio:SIO_001121
.
}
dgn-np:NP440249.RAcBDz1_lgtSnEj-p5JadAJ8002Unu2MAZlvq_J9UWEe4130_provenance
{
dgn-np:NP440249.RAcBDz1_lgtSnEj-p5JadAJ8002Unu2MAZlvq_J9UWEe4130_assertion
dcterms:description
"[These observations suggest that RARS-T is indeed a myeloid neoplasm with both myelodysplastic and myeloproliferative features at the molecular and clinical levels and that it may develop from RARS through the acquisition of somatic mutations of JAK2, MPL, or other as-yet-unknown genes.]. 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:19692701
;
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:NP440249.RAcBDz1_lgtSnEj-p5JadAJ8002Unu2MAZlvq_J9UWEe4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:20+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" .
}