@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP452356.RAqK1l46an9BxgJ4zhpJg-K83QcsQWJYLF3w4Tw44VZ4g
> .
@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:NP452356.RAqK1l46an9BxgJ4zhpJg-K83QcsQWJYLF3w4Tw44VZ4g130_head
{
this:
np:hasAssertion
dgn-np:NP452356.RAqK1l46an9BxgJ4zhpJg-K83QcsQWJYLF3w4Tw44VZ4g130_assertion
;
np:hasProvenance
dgn-np:NP452356.RAqK1l46an9BxgJ4zhpJg-K83QcsQWJYLF3w4Tw44VZ4g130_provenance
;
np:hasPublicationInfo
dgn-np:NP452356.RAqK1l46an9BxgJ4zhpJg-K83QcsQWJYLF3w4Tw44VZ4g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP452356.RAqK1l46an9BxgJ4zhpJg-K83QcsQWJYLF3w4Tw44VZ4g130_assertion
a
np:Assertion
.
dgn-np:NP452356.RAqK1l46an9BxgJ4zhpJg-K83QcsQWJYLF3w4Tw44VZ4g130_provenance
a
np:Provenance
.
dgn-np:NP452356.RAqK1l46an9BxgJ4zhpJg-K83QcsQWJYLF3w4Tw44VZ4g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP452356.RAqK1l46an9BxgJ4zhpJg-K83QcsQWJYLF3w4Tw44VZ4g130_assertion
{
miriam-gene:4893
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGNa8a19c1f72e67eb29dcf567cb6951c6b
sio:SIO_000628
miriam-gene:4893
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP452356.RAqK1l46an9BxgJ4zhpJg-K83QcsQWJYLF3w4Tw44VZ4g130_provenance
{
dgn-np:NP452356.RAqK1l46an9BxgJ4zhpJg-K83QcsQWJYLF3w4Tw44VZ4g130_assertion
dcterms:description
"[Mutations of the NRAS and TP53 genes and internal tandem duplication (ITD) of the FLT3 gene are among the most frequently observed molecular abnormalities in the myelodysplastic syndromes (MDS) and acute myeloid leukemia (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:15257941
;
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:NP452356.RAqK1l46an9BxgJ4zhpJg-K83QcsQWJYLF3w4Tw44VZ4g130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:10+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" .
}