@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP222883.RAgThmJTTvbTAuPPXCWa81oE_rwSCZg7x8a8hp0FV31wk
> .
@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:NP222883.RAgThmJTTvbTAuPPXCWa81oE_rwSCZg7x8a8hp0FV31wk130_head
{
this:
np:hasAssertion
dgn-np:NP222883.RAgThmJTTvbTAuPPXCWa81oE_rwSCZg7x8a8hp0FV31wk130_assertion
;
np:hasProvenance
dgn-np:NP222883.RAgThmJTTvbTAuPPXCWa81oE_rwSCZg7x8a8hp0FV31wk130_provenance
;
np:hasPublicationInfo
dgn-np:NP222883.RAgThmJTTvbTAuPPXCWa81oE_rwSCZg7x8a8hp0FV31wk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP222883.RAgThmJTTvbTAuPPXCWa81oE_rwSCZg7x8a8hp0FV31wk130_assertion
a
np:Assertion
.
dgn-np:NP222883.RAgThmJTTvbTAuPPXCWa81oE_rwSCZg7x8a8hp0FV31wk130_provenance
a
np:Provenance
.
dgn-np:NP222883.RAgThmJTTvbTAuPPXCWa81oE_rwSCZg7x8a8hp0FV31wk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP222883.RAgThmJTTvbTAuPPXCWa81oE_rwSCZg7x8a8hp0FV31wk130_assertion
{
miriam-gene:4791
a
ncit:C16612
.
lld:C0026764
a
ncit:C7057
.
dgn-gda:DGNf57d4ea4846e923ded9e6232c9286a42
sio:SIO_000628
miriam-gene:4791
,
lld:C0026764
;
a
sio:SIO_001121
.
}
dgn-np:NP222883.RAgThmJTTvbTAuPPXCWa81oE_rwSCZg7x8a8hp0FV31wk130_provenance
{
dgn-np:NP222883.RAgThmJTTvbTAuPPXCWa81oE_rwSCZg7x8a8hp0FV31wk130_assertion
dcterms:description
"[In one case of multiple myeloma (MM), cloning and sequencing analysis of reciprocal breakpoint sites showed that they occurred within intron 15 of the NFKB2 gene and led to the complete deletion of the 3' portion of the gene coding for the ankyrin domain.]. 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:7949142
;
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:NP222883.RAgThmJTTvbTAuPPXCWa81oE_rwSCZg7x8a8hp0FV31wk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:03+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" .
}