@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP496754.RAAEQ8B0lYnx-eVjm8isMx7z_PnsfuiTLOxsx0iiZaEss
> .
@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:NP496754.RAAEQ8B0lYnx-eVjm8isMx7z_PnsfuiTLOxsx0iiZaEss130_head
{
this:
np:hasAssertion
dgn-np:NP496754.RAAEQ8B0lYnx-eVjm8isMx7z_PnsfuiTLOxsx0iiZaEss130_assertion
;
np:hasProvenance
dgn-np:NP496754.RAAEQ8B0lYnx-eVjm8isMx7z_PnsfuiTLOxsx0iiZaEss130_provenance
;
np:hasPublicationInfo
dgn-np:NP496754.RAAEQ8B0lYnx-eVjm8isMx7z_PnsfuiTLOxsx0iiZaEss130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP496754.RAAEQ8B0lYnx-eVjm8isMx7z_PnsfuiTLOxsx0iiZaEss130_assertion
a
np:Assertion
.
dgn-np:NP496754.RAAEQ8B0lYnx-eVjm8isMx7z_PnsfuiTLOxsx0iiZaEss130_provenance
a
np:Provenance
.
dgn-np:NP496754.RAAEQ8B0lYnx-eVjm8isMx7z_PnsfuiTLOxsx0iiZaEss130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP496754.RAAEQ8B0lYnx-eVjm8isMx7z_PnsfuiTLOxsx0iiZaEss130_assertion
{
miriam-gene:4609
a
ncit:C16612
.
lld:C0598766
a
ncit:C7057
.
dgn-gda:DGNa84e1c63b8f24810a0bde8a71d76576c
sio:SIO_000628
miriam-gene:4609
,
lld:C0598766
;
a
sio:SIO_001121
.
}
dgn-np:NP496754.RAAEQ8B0lYnx-eVjm8isMx7z_PnsfuiTLOxsx0iiZaEss130_provenance
{
dgn-np:NP496754.RAAEQ8B0lYnx-eVjm8isMx7z_PnsfuiTLOxsx0iiZaEss130_assertion
dcterms:description
"[These results indicate an IGL-mediated rearrangement of an unknown gene at 9q34 that together with BCL2 and MYC might be involved in the lymphomagenesis of the present case of FCCL and perhaps in other cases of non-Hodgkin lymphoma in which t(9;22) is sporadically occurring.]. 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:9331562
;
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:NP496754.RAAEQ8B0lYnx-eVjm8isMx7z_PnsfuiTLOxsx0iiZaEss130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:56+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
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