@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP824893.RAaHGsZlUWKqAJYEBdoh5vtfLvBg6-NOihR2QRWyIdI5M
> .
@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:NP824893.RAaHGsZlUWKqAJYEBdoh5vtfLvBg6-NOihR2QRWyIdI5M130_head
{
this:
np:hasAssertion
dgn-np:NP824893.RAaHGsZlUWKqAJYEBdoh5vtfLvBg6-NOihR2QRWyIdI5M130_assertion
;
np:hasProvenance
dgn-np:NP824893.RAaHGsZlUWKqAJYEBdoh5vtfLvBg6-NOihR2QRWyIdI5M130_provenance
;
np:hasPublicationInfo
dgn-np:NP824893.RAaHGsZlUWKqAJYEBdoh5vtfLvBg6-NOihR2QRWyIdI5M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP824893.RAaHGsZlUWKqAJYEBdoh5vtfLvBg6-NOihR2QRWyIdI5M130_assertion
a
np:Assertion
.
dgn-np:NP824893.RAaHGsZlUWKqAJYEBdoh5vtfLvBg6-NOihR2QRWyIdI5M130_provenance
a
np:Provenance
.
dgn-np:NP824893.RAaHGsZlUWKqAJYEBdoh5vtfLvBg6-NOihR2QRWyIdI5M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP824893.RAaHGsZlUWKqAJYEBdoh5vtfLvBg6-NOihR2QRWyIdI5M130_assertion
{
miriam-gene:4928
a
ncit:C16612
.
lld:C0220621
a
ncit:C7057
.
dgn-gda:DGNa00a4405ff9f40cddf551f2687053e6c
sio:SIO_000628
miriam-gene:4928
,
lld:C0220621
;
a
sio:SIO_001121
.
}
dgn-np:NP824893.RAaHGsZlUWKqAJYEBdoh5vtfLvBg6-NOihR2QRWyIdI5M130_provenance
{
dgn-np:NP824893.RAaHGsZlUWKqAJYEBdoh5vtfLvBg6-NOihR2QRWyIdI5M130_assertion
dcterms:description
"[The aim of this study was to determine the incidence of rearrangements of NUP98 (the gene coding for nucleoporin 98kDa protein) in childhood acute myeloid leukemia (AML) and selected patients with 11p13-15 rearrangements.]. 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:15951287
;
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:NP824893.RAaHGsZlUWKqAJYEBdoh5vtfLvBg6-NOihR2QRWyIdI5M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:25+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" .
}