@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP363928.RAK3AdjaE5fFTi5uOSTgcrzWzE9ypPHhERjaWuV2nkR50
> .
@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:NP363928.RAK3AdjaE5fFTi5uOSTgcrzWzE9ypPHhERjaWuV2nkR50130_head
{
this:
np:hasAssertion
dgn-np:NP363928.RAK3AdjaE5fFTi5uOSTgcrzWzE9ypPHhERjaWuV2nkR50130_assertion
;
np:hasProvenance
dgn-np:NP363928.RAK3AdjaE5fFTi5uOSTgcrzWzE9ypPHhERjaWuV2nkR50130_provenance
;
np:hasPublicationInfo
dgn-np:NP363928.RAK3AdjaE5fFTi5uOSTgcrzWzE9ypPHhERjaWuV2nkR50130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP363928.RAK3AdjaE5fFTi5uOSTgcrzWzE9ypPHhERjaWuV2nkR50130_assertion
a
np:Assertion
.
dgn-np:NP363928.RAK3AdjaE5fFTi5uOSTgcrzWzE9ypPHhERjaWuV2nkR50130_provenance
a
np:Provenance
.
dgn-np:NP363928.RAK3AdjaE5fFTi5uOSTgcrzWzE9ypPHhERjaWuV2nkR50130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP363928.RAK3AdjaE5fFTi5uOSTgcrzWzE9ypPHhERjaWuV2nkR50130_assertion
{
miriam-gene:4609
a
ncit:C16612
.
lld:C0023434
a
ncit:C7057
.
dgn-gda:DGNbcf2021a8c8b3b546bb7e8d62e90aeca
sio:SIO_000628
miriam-gene:4609
,
lld:C0023434
;
a
sio:SIO_001121
.
}
dgn-np:NP363928.RAK3AdjaE5fFTi5uOSTgcrzWzE9ypPHhERjaWuV2nkR50130_provenance
{
dgn-np:NP363928.RAK3AdjaE5fFTi5uOSTgcrzWzE9ypPHhERjaWuV2nkR50130_assertion
dcterms:description
"[The rarity of t(8;14) in CLL together with a cryptic deletion that probably includes the MYC gene in our CLL patient persuaded us to explore the clinicopathological role of MYC translocations by comparing disease progression in our patient and in other reported CLL cases.]. 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:16616107
;
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:NP363928.RAK3AdjaE5fFTi5uOSTgcrzWzE9ypPHhERjaWuV2nkR50130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:33+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" .
}