@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP306930.RATW75DIQzkfjrPPA3BpU-_vt5kWQK0MpKIyBinE4vPL4
> .
@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:NP306930.RATW75DIQzkfjrPPA3BpU-_vt5kWQK0MpKIyBinE4vPL4130_head
{
this:
np:hasAssertion
dgn-np:NP306930.RATW75DIQzkfjrPPA3BpU-_vt5kWQK0MpKIyBinE4vPL4130_assertion
;
np:hasProvenance
dgn-np:NP306930.RATW75DIQzkfjrPPA3BpU-_vt5kWQK0MpKIyBinE4vPL4130_provenance
;
np:hasPublicationInfo
dgn-np:NP306930.RATW75DIQzkfjrPPA3BpU-_vt5kWQK0MpKIyBinE4vPL4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP306930.RATW75DIQzkfjrPPA3BpU-_vt5kWQK0MpKIyBinE4vPL4130_assertion
a
np:Assertion
.
dgn-np:NP306930.RATW75DIQzkfjrPPA3BpU-_vt5kWQK0MpKIyBinE4vPL4130_provenance
a
np:Provenance
.
dgn-np:NP306930.RATW75DIQzkfjrPPA3BpU-_vt5kWQK0MpKIyBinE4vPL4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP306930.RATW75DIQzkfjrPPA3BpU-_vt5kWQK0MpKIyBinE4vPL4130_assertion
{
miriam-gene:2322
a
ncit:C16612
.
lld:C2697636
a
ncit:C7057
.
dgn-gda:DGNb0939ae84281b7c915c8584673e17e18
sio:SIO_000628
miriam-gene:2322
,
lld:C2697636
;
a
sio:SIO_001121
.
}
dgn-np:NP306930.RATW75DIQzkfjrPPA3BpU-_vt5kWQK0MpKIyBinE4vPL4130_provenance
{
dgn-np:NP306930.RATW75DIQzkfjrPPA3BpU-_vt5kWQK0MpKIyBinE4vPL4130_assertion
dcterms:description
"[As known activating FLT3 mutations are often absent in these patients, we screened the entire FLT3 coding sequence in MLL rearranged and hyperdiploid ALL cases for yet unidentified additional genetic alterations using denaturing D-HPLC.]. 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:18024407
;
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:NP306930.RATW75DIQzkfjrPPA3BpU-_vt5kWQK0MpKIyBinE4vPL4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:56+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" .
}