@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP319529.RAHpYT3SuJJpaRw79H-wMarWj2txp0Ylb8UQ5m6YQ5LUc
> .
@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:NP319529.RAHpYT3SuJJpaRw79H-wMarWj2txp0Ylb8UQ5m6YQ5LUc130_head
{
this:
np:hasAssertion
dgn-np:NP319529.RAHpYT3SuJJpaRw79H-wMarWj2txp0Ylb8UQ5m6YQ5LUc130_assertion
;
np:hasProvenance
dgn-np:NP319529.RAHpYT3SuJJpaRw79H-wMarWj2txp0Ylb8UQ5m6YQ5LUc130_provenance
;
np:hasPublicationInfo
dgn-np:NP319529.RAHpYT3SuJJpaRw79H-wMarWj2txp0Ylb8UQ5m6YQ5LUc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP319529.RAHpYT3SuJJpaRw79H-wMarWj2txp0Ylb8UQ5m6YQ5LUc130_assertion
a
np:Assertion
.
dgn-np:NP319529.RAHpYT3SuJJpaRw79H-wMarWj2txp0Ylb8UQ5m6YQ5LUc130_provenance
a
np:Provenance
.
dgn-np:NP319529.RAHpYT3SuJJpaRw79H-wMarWj2txp0Ylb8UQ5m6YQ5LUc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP319529.RAHpYT3SuJJpaRw79H-wMarWj2txp0Ylb8UQ5m6YQ5LUc130_assertion
{
miriam-gene:7294
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN6094d2fc4d6299b6d4c5bc756045b54b
sio:SIO_000628
miriam-gene:7294
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP319529.RAHpYT3SuJJpaRw79H-wMarWj2txp0Ylb8UQ5m6YQ5LUc130_provenance
{
dgn-np:NP319529.RAHpYT3SuJJpaRw79H-wMarWj2txp0Ylb8UQ5m6YQ5LUc130_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:NP319529.RAHpYT3SuJJpaRw79H-wMarWj2txp0Ylb8UQ5m6YQ5LUc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:05+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" .
}