@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP916494.RAxOMbIUsEEq1xggxPCVPVHAH3FDPkE7pfL6wdIgqsJeQ
> .
@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:NP916494.RAxOMbIUsEEq1xggxPCVPVHAH3FDPkE7pfL6wdIgqsJeQ130_head
{
this:
np:hasAssertion
dgn-np:NP916494.RAxOMbIUsEEq1xggxPCVPVHAH3FDPkE7pfL6wdIgqsJeQ130_assertion
;
np:hasProvenance
dgn-np:NP916494.RAxOMbIUsEEq1xggxPCVPVHAH3FDPkE7pfL6wdIgqsJeQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP916494.RAxOMbIUsEEq1xggxPCVPVHAH3FDPkE7pfL6wdIgqsJeQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP916494.RAxOMbIUsEEq1xggxPCVPVHAH3FDPkE7pfL6wdIgqsJeQ130_assertion
a
np:Assertion
.
dgn-np:NP916494.RAxOMbIUsEEq1xggxPCVPVHAH3FDPkE7pfL6wdIgqsJeQ130_provenance
a
np:Provenance
.
dgn-np:NP916494.RAxOMbIUsEEq1xggxPCVPVHAH3FDPkE7pfL6wdIgqsJeQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP916494.RAxOMbIUsEEq1xggxPCVPVHAH3FDPkE7pfL6wdIgqsJeQ130_assertion
{
miriam-gene:7294
a
ncit:C16612
.
lld:C0023449
a
ncit:C7057
.
dgn-gda:DGN532a2974f7c9e97bf0a27bf3ef833451
sio:SIO_000628
miriam-gene:7294
,
lld:C0023449
;
a
sio:SIO_001121
.
}
dgn-np:NP916494.RAxOMbIUsEEq1xggxPCVPVHAH3FDPkE7pfL6wdIgqsJeQ130_provenance
{
dgn-np:NP916494.RAxOMbIUsEEq1xggxPCVPVHAH3FDPkE7pfL6wdIgqsJeQ130_assertion
dcterms:description
"[Activating FLT3 mutations are the most common genetic aberrations in acute myeloid leukemia (AML), resulting in the constitutive activation of this receptor tyrosine kinase (RTK), but such mutations are rarely found in acute lymphoblastic leukemia (ALL).]. 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:15044257
;
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:NP916494.RAxOMbIUsEEq1xggxPCVPVHAH3FDPkE7pfL6wdIgqsJeQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:22+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" .
}