@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP242037.RAu_VhA0LyVRqOvEAztKQz-nlBFKSAkHI8dBfiP8OH04E
> .
@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:NP242037.RAu_VhA0LyVRqOvEAztKQz-nlBFKSAkHI8dBfiP8OH04E130_head
{
this:
np:hasAssertion
dgn-np:NP242037.RAu_VhA0LyVRqOvEAztKQz-nlBFKSAkHI8dBfiP8OH04E130_assertion
;
np:hasProvenance
dgn-np:NP242037.RAu_VhA0LyVRqOvEAztKQz-nlBFKSAkHI8dBfiP8OH04E130_provenance
;
np:hasPublicationInfo
dgn-np:NP242037.RAu_VhA0LyVRqOvEAztKQz-nlBFKSAkHI8dBfiP8OH04E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP242037.RAu_VhA0LyVRqOvEAztKQz-nlBFKSAkHI8dBfiP8OH04E130_assertion
a
np:Assertion
.
dgn-np:NP242037.RAu_VhA0LyVRqOvEAztKQz-nlBFKSAkHI8dBfiP8OH04E130_provenance
a
np:Provenance
.
dgn-np:NP242037.RAu_VhA0LyVRqOvEAztKQz-nlBFKSAkHI8dBfiP8OH04E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP242037.RAu_VhA0LyVRqOvEAztKQz-nlBFKSAkHI8dBfiP8OH04E130_assertion
{
miriam-gene:7301
a
ncit:C16612
.
lld:C0023449
a
ncit:C7057
.
dgn-gda:DGN21047f2325719c58dad99f829e5ed8ed
sio:SIO_000628
miriam-gene:7301
,
lld:C0023449
;
a
sio:SIO_001121
.
}
dgn-np:NP242037.RAu_VhA0LyVRqOvEAztKQz-nlBFKSAkHI8dBfiP8OH04E130_provenance
{
dgn-np:NP242037.RAu_VhA0LyVRqOvEAztKQz-nlBFKSAkHI8dBfiP8OH04E130_assertion
dcterms:description
"[Spectral karyotyping (SKY) on metaphase spreads from 15 high hyperdiploid (>51 chromosomes) childhood acute lymphoblastic leukemias (ALL), which typically display a poor chromosome morphology, was performed in order to investigate the pattern of numerical abnormalities, reveal the chromosomal origin of marker chromosomes, and identify translocations and other interchromosomal rearrangements not detected by G-banding analysis.]. 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:11422408
;
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:NP242037.RAu_VhA0LyVRqOvEAztKQz-nlBFKSAkHI8dBfiP8OH04E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:15+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" .
}