@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP286810.RAeEpE1gWnYKwCYXC-rWvO_lgM1rLE215zMW72GMQMju0
> .
@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:NP286810.RAeEpE1gWnYKwCYXC-rWvO_lgM1rLE215zMW72GMQMju0130_head
{
this:
np:hasAssertion
dgn-np:NP286810.RAeEpE1gWnYKwCYXC-rWvO_lgM1rLE215zMW72GMQMju0130_assertion
;
np:hasProvenance
dgn-np:NP286810.RAeEpE1gWnYKwCYXC-rWvO_lgM1rLE215zMW72GMQMju0130_provenance
;
np:hasPublicationInfo
dgn-np:NP286810.RAeEpE1gWnYKwCYXC-rWvO_lgM1rLE215zMW72GMQMju0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP286810.RAeEpE1gWnYKwCYXC-rWvO_lgM1rLE215zMW72GMQMju0130_assertion
a
np:Assertion
.
dgn-np:NP286810.RAeEpE1gWnYKwCYXC-rWvO_lgM1rLE215zMW72GMQMju0130_provenance
a
np:Provenance
.
dgn-np:NP286810.RAeEpE1gWnYKwCYXC-rWvO_lgM1rLE215zMW72GMQMju0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP286810.RAeEpE1gWnYKwCYXC-rWvO_lgM1rLE215zMW72GMQMju0130_assertion
{
miriam-gene:7301
a
ncit:C16612
.
lld:C3463824
a
ncit:C7057
.
dgn-gda:DGN5748a24ad3567c88a23c76e1177c34a0
sio:SIO_000628
miriam-gene:7301
,
lld:C3463824
;
a
sio:SIO_001121
.
}
dgn-np:NP286810.RAeEpE1gWnYKwCYXC-rWvO_lgM1rLE215zMW72GMQMju0130_provenance
{
dgn-np:NP286810.RAeEpE1gWnYKwCYXC-rWvO_lgM1rLE215zMW72GMQMju0130_assertion
dcterms:description
"[To obtain a more comprehensive view of the recurrent aberrations, we performed spectral karyotyping (SKY) and fluorescence in situ hybridization (FISH) with selected probes on bone marrow samples from 17 patients with primary MDS and 3 with primary AML.]. 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:16490597
;
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:NP286810.RAeEpE1gWnYKwCYXC-rWvO_lgM1rLE215zMW72GMQMju0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:43+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" .
}