@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP168424.RAqxJETAT2NLbGf7EA1hHy_pBtWjLGAns53Ib4YUSUD24
> .
@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:NP168424.RAqxJETAT2NLbGf7EA1hHy_pBtWjLGAns53Ib4YUSUD24130_head
{
this:
np:hasAssertion
dgn-np:NP168424.RAqxJETAT2NLbGf7EA1hHy_pBtWjLGAns53Ib4YUSUD24130_assertion
;
np:hasProvenance
dgn-np:NP168424.RAqxJETAT2NLbGf7EA1hHy_pBtWjLGAns53Ib4YUSUD24130_provenance
;
np:hasPublicationInfo
dgn-np:NP168424.RAqxJETAT2NLbGf7EA1hHy_pBtWjLGAns53Ib4YUSUD24130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP168424.RAqxJETAT2NLbGf7EA1hHy_pBtWjLGAns53Ib4YUSUD24130_assertion
a
np:Assertion
.
dgn-np:NP168424.RAqxJETAT2NLbGf7EA1hHy_pBtWjLGAns53Ib4YUSUD24130_provenance
a
np:Provenance
.
dgn-np:NP168424.RAqxJETAT2NLbGf7EA1hHy_pBtWjLGAns53Ib4YUSUD24130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP168424.RAqxJETAT2NLbGf7EA1hHy_pBtWjLGAns53Ib4YUSUD24130_assertion
{
miriam-gene:6003
a
ncit:C16612
.
lld:C0041107
a
ncit:C7057
.
dgn-gda:DGN06d266bcb7fa2d2532be9f6ddcb52e80
sio:SIO_000628
miriam-gene:6003
,
lld:C0041107
;
a
sio:SIO_001121
.
}
dgn-np:NP168424.RAqxJETAT2NLbGf7EA1hHy_pBtWjLGAns53Ib4YUSUD24130_provenance
{
dgn-np:NP168424.RAqxJETAT2NLbGf7EA1hHy_pBtWjLGAns53Ib4YUSUD24130_assertion
dcterms:description
"[By analyzing several genes with very high (`spiked`) expression in individual cases, we identified clusters with different biologic characteristics, such as samples with MALT1 translocations having high expression of MALT1 and RARA, samples with plasmacytic differentiation having high FKBP11 expression, and samples with high RGS13 expression tending to have trisomy 3 and reactive follicles.]. 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:18974375
;
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:NP168424.RAqxJETAT2NLbGf7EA1hHy_pBtWjLGAns53Ib4YUSUD24130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:31+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" .
}