@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP127464.RA8llxKBtgwusQmbDxuBsgFGt-1ZdovEfGGqVd-orXzag
> .
@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:NP127464.RA8llxKBtgwusQmbDxuBsgFGt-1ZdovEfGGqVd-orXzag130_head
{
this:
np:hasAssertion
dgn-np:NP127464.RA8llxKBtgwusQmbDxuBsgFGt-1ZdovEfGGqVd-orXzag130_assertion
;
np:hasProvenance
dgn-np:NP127464.RA8llxKBtgwusQmbDxuBsgFGt-1ZdovEfGGqVd-orXzag130_provenance
;
np:hasPublicationInfo
dgn-np:NP127464.RA8llxKBtgwusQmbDxuBsgFGt-1ZdovEfGGqVd-orXzag130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP127464.RA8llxKBtgwusQmbDxuBsgFGt-1ZdovEfGGqVd-orXzag130_assertion
a
np:Assertion
.
dgn-np:NP127464.RA8llxKBtgwusQmbDxuBsgFGt-1ZdovEfGGqVd-orXzag130_provenance
a
np:Provenance
.
dgn-np:NP127464.RA8llxKBtgwusQmbDxuBsgFGt-1ZdovEfGGqVd-orXzag130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP127464.RA8llxKBtgwusQmbDxuBsgFGt-1ZdovEfGGqVd-orXzag130_assertion
{
miriam-gene:2322
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGNb671fdc31ebbde3921f2ac5e462550a3
sio:SIO_000628
miriam-gene:2322
,
lld:C0023418
;
a
sio:SIO_001122
.
}
dgn-np:NP127464.RA8llxKBtgwusQmbDxuBsgFGt-1ZdovEfGGqVd-orXzag130_provenance
{
dgn-np:NP127464.RA8llxKBtgwusQmbDxuBsgFGt-1ZdovEfGGqVd-orXzag130_assertion
dcterms:description
"[A high-throughput platform was used to interrogate the entire FLT3 coding sequence in Leukemia, Monocytic, Acute patients without known FLT3 mutations and the consequences of each candidate leukemogenic allele was experimentally tested.]. 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:18068628
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP127464.RA8llxKBtgwusQmbDxuBsgFGt-1ZdovEfGGqVd-orXzag130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:06+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" .
}