@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP817421.RABZTS_wbYMy3F5DuH_hx4REilC2pDi2BZZgPmvrz2oew
> .
@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:NP817421.RABZTS_wbYMy3F5DuH_hx4REilC2pDi2BZZgPmvrz2oew130_head
{
this:
np:hasAssertion
dgn-np:NP817421.RABZTS_wbYMy3F5DuH_hx4REilC2pDi2BZZgPmvrz2oew130_assertion
;
np:hasProvenance
dgn-np:NP817421.RABZTS_wbYMy3F5DuH_hx4REilC2pDi2BZZgPmvrz2oew130_provenance
;
np:hasPublicationInfo
dgn-np:NP817421.RABZTS_wbYMy3F5DuH_hx4REilC2pDi2BZZgPmvrz2oew130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP817421.RABZTS_wbYMy3F5DuH_hx4REilC2pDi2BZZgPmvrz2oew130_assertion
a
np:Assertion
.
dgn-np:NP817421.RABZTS_wbYMy3F5DuH_hx4REilC2pDi2BZZgPmvrz2oew130_provenance
a
np:Provenance
.
dgn-np:NP817421.RABZTS_wbYMy3F5DuH_hx4REilC2pDi2BZZgPmvrz2oew130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP817421.RABZTS_wbYMy3F5DuH_hx4REilC2pDi2BZZgPmvrz2oew130_assertion
{
miriam-gene:4914
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN94069f854cfa2111764bb85970762bf1
sio:SIO_000628
miriam-gene:4914
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP817421.RABZTS_wbYMy3F5DuH_hx4REilC2pDi2BZZgPmvrz2oew130_provenance
{
dgn-np:NP817421.RABZTS_wbYMy3F5DuH_hx4REilC2pDi2BZZgPmvrz2oew130_assertion
dcterms:description
"[The tyrosine kinase receptor Flt3 (Fms-like tyrosine kinase 3) is almost always expressed in AML (acute myeloid leukemia) cells, and constitutive activation of Flt3 by ITD (internal tandem duplication) mutations is one of the most common molecular alterations known in AML, especially monocytic 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:23017497
;
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:NP817421.RABZTS_wbYMy3F5DuH_hx4REilC2pDi2BZZgPmvrz2oew130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:21+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" .
}