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http://rdf.disgenet.org/nanopublications.trig#NP495167.RAnic60PmQvEhpCtzaBWSKfcDO6HPMTfbJfxeCaz9wCUo
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
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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#
> .
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{
this:
np:hasAssertion
dgn-np:NP495167.RAnic60PmQvEhpCtzaBWSKfcDO6HPMTfbJfxeCaz9wCUo130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP495167.RAnic60PmQvEhpCtzaBWSKfcDO6HPMTfbJfxeCaz9wCUo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP495167.RAnic60PmQvEhpCtzaBWSKfcDO6HPMTfbJfxeCaz9wCUo130_assertion
a
np:Assertion
.
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a
np:Provenance
.
dgn-np:NP495167.RAnic60PmQvEhpCtzaBWSKfcDO6HPMTfbJfxeCaz9wCUo130_publicationInfo
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np:PublicationInfo
.
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{
miriam-gene:10934
a
ncit:C16612
.
lld:C0024419
a
ncit:C7057
.
dgn-gda:DGNd222ed02aec3265e06c6cca4ee9b9a8c
sio:SIO_000628
miriam-gene:10934
,
lld:C0024419
;
a
sio:SIO_001121
.
}
dgn-np:NP495167.RAnic60PmQvEhpCtzaBWSKfcDO6HPMTfbJfxeCaz9wCUo130_provenance
{
dgn-np:NP495167.RAnic60PmQvEhpCtzaBWSKfcDO6HPMTfbJfxeCaz9wCUo130_assertion
dcterms:description
"[However, we found that the mutation of switch regions essential for CSR were present in IgM monoclonal gammopathy of unknown significance (MGUS) but absent from WM B cells, suggesting the possibility that not all IgM MGUS have the potential to give rise to WM, and further strengthening the hypothesis that the target cell in transformation to WM is an unusual type of B cell.]. 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:15794851
;
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 .
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dgn-np:NP495167.RAnic60PmQvEhpCtzaBWSKfcDO6HPMTfbJfxeCaz9wCUo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:55+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
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> , <
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> , <
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> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
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