@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP298687.RAprnN9fcIWle88CGF4gs2KFjncBqASirEckvUAMBhIpk
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP298687.RAprnN9fcIWle88CGF4gs2KFjncBqASirEckvUAMBhIpk130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP298687.RAprnN9fcIWle88CGF4gs2KFjncBqASirEckvUAMBhIpk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP298687.RAprnN9fcIWle88CGF4gs2KFjncBqASirEckvUAMBhIpk130_assertion
a
np:Assertion
.
dgn-np:NP298687.RAprnN9fcIWle88CGF4gs2KFjncBqASirEckvUAMBhIpk130_provenance
a
np:Provenance
.
dgn-np:NP298687.RAprnN9fcIWle88CGF4gs2KFjncBqASirEckvUAMBhIpk130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:4928
a
ncit:C16612
.
lld:C0026986
a
ncit:C7057
.
dgn-gda:DGN7f962d7d8469eea07eda64f5bb22ab41
sio:SIO_000628
miriam-gene:4928
,
lld:C0026986
;
a
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.
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dgn-np:NP298687.RAprnN9fcIWle88CGF4gs2KFjncBqASirEckvUAMBhIpk130_provenance
{
dgn-np:NP298687.RAprnN9fcIWle88CGF4gs2KFjncBqASirEckvUAMBhIpk130_assertion
dcterms:description
"[Using a NUP98-specific split-signal fluorescence in situ hybridization (FISH) probe combination, we analyzed 84 patients with acute myeloid leukemia (AML), acute lymphoblastic leukemia, or myelodysplastic syndrome with either normal karyotypes or 11p abnormalities to investigate whether there are unidentified 11p15 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:16419055
;
prov:wasDerivedFrom
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;
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 .
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dgn-np:NP298687.RAprnN9fcIWle88CGF4gs2KFjncBqASirEckvUAMBhIpk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:49+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
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pav:authoredBy
<
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> , <
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> , <
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> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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