@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP458762.RA1a_KboNyQ4qo5agPuSPhW9gJq_Q5u2h5uHnouTDTOgI
> .
@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:NP458762.RA1a_KboNyQ4qo5agPuSPhW9gJq_Q5u2h5uHnouTDTOgI130_head
{
this:
np:hasAssertion
dgn-np:NP458762.RA1a_KboNyQ4qo5agPuSPhW9gJq_Q5u2h5uHnouTDTOgI130_assertion
;
np:hasProvenance
dgn-np:NP458762.RA1a_KboNyQ4qo5agPuSPhW9gJq_Q5u2h5uHnouTDTOgI130_provenance
;
np:hasPublicationInfo
dgn-np:NP458762.RA1a_KboNyQ4qo5agPuSPhW9gJq_Q5u2h5uHnouTDTOgI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP458762.RA1a_KboNyQ4qo5agPuSPhW9gJq_Q5u2h5uHnouTDTOgI130_assertion
a
np:Assertion
.
dgn-np:NP458762.RA1a_KboNyQ4qo5agPuSPhW9gJq_Q5u2h5uHnouTDTOgI130_provenance
a
np:Provenance
.
dgn-np:NP458762.RA1a_KboNyQ4qo5agPuSPhW9gJq_Q5u2h5uHnouTDTOgI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP458762.RA1a_KboNyQ4qo5agPuSPhW9gJq_Q5u2h5uHnouTDTOgI130_assertion
{
miriam-gene:6520
a
ncit:C16612
.
lld:C0026470
a
ncit:C7057
.
dgn-gda:DGNdf6ac87809623cb61acc9a28203f841b
sio:SIO_000628
miriam-gene:6520
,
lld:C0026470
;
a
sio:SIO_001121
.
}
dgn-np:NP458762.RA1a_KboNyQ4qo5agPuSPhW9gJq_Q5u2h5uHnouTDTOgI130_provenance
{
dgn-np:NP458762.RA1a_KboNyQ4qo5agPuSPhW9gJq_Q5u2h5uHnouTDTOgI130_assertion
dcterms:description
"[Chromosome 13 deletion (Delta13), deletion of TP53, ploidy status and immunoglobulin heavy chain (IgH) translocations were evaluated by fluorescence in situ hybridization in patients with monoclonal gammopathy of undetermined significance (n=189), smoldering multiple myeloma (n=127) and multiple myeloma (n=400).]. 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:19996118
;
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:NP458762.RA1a_KboNyQ4qo5agPuSPhW9gJq_Q5u2h5uHnouTDTOgI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:33+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" .
}