@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1122654.RAZya8GAXNPwrFkw17NlhNlO48s76tUdd6LGIuiCKq5EA
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1122654.RAZya8GAXNPwrFkw17NlhNlO48s76tUdd6LGIuiCKq5EA130_head
{
this:
np:hasAssertion
dgn-np:NP1122654.RAZya8GAXNPwrFkw17NlhNlO48s76tUdd6LGIuiCKq5EA130_assertion
;
np:hasProvenance
dgn-np:NP1122654.RAZya8GAXNPwrFkw17NlhNlO48s76tUdd6LGIuiCKq5EA130_provenance
;
np:hasPublicationInfo
dgn-np:NP1122654.RAZya8GAXNPwrFkw17NlhNlO48s76tUdd6LGIuiCKq5EA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1122654.RAZya8GAXNPwrFkw17NlhNlO48s76tUdd6LGIuiCKq5EA130_assertion
a
np:Assertion
.
dgn-np:NP1122654.RAZya8GAXNPwrFkw17NlhNlO48s76tUdd6LGIuiCKq5EA130_provenance
a
np:Provenance
.
dgn-np:NP1122654.RAZya8GAXNPwrFkw17NlhNlO48s76tUdd6LGIuiCKq5EA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1122654.RAZya8GAXNPwrFkw17NlhNlO48s76tUdd6LGIuiCKq5EA130_assertion
{
miriam-gene:8764
a
ncit:C16612
.
lld:C0024301
a
ncit:C7057
.
dgn-gda:DGN45b1fb2ba1aacd25760b99c4fba6e38d
sio:SIO_000628
miriam-gene:8764
,
lld:C0024301
;
a
sio:SIO_001121
.
}
dgn-np:NP1122654.RAZya8GAXNPwrFkw17NlhNlO48s76tUdd6LGIuiCKq5EA130_provenance
{
dgn-np:NP1122654.RAZya8GAXNPwrFkw17NlhNlO48s76tUdd6LGIuiCKq5EA130_assertion
dcterms:description
"[Among the most notable alterations, we observed and validated deletions of 1p36 and gains of the 7p and 12q chromosomes and related oncogenes, which include some of the most recurrent oncogenic alterations in overt follicular lymphoma (TNFRSF14, EZH2, MLL2).]. 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:24162788
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1122654.RAZya8GAXNPwrFkw17NlhNlO48s76tUdd6LGIuiCKq5EA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:15+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}