@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP207177.RALB-Za9DfRE4_5k4PCE3KfEW40BCZrrQbYKoP8MU7hQ0
> .
@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:NP207177.RALB-Za9DfRE4_5k4PCE3KfEW40BCZrrQbYKoP8MU7hQ0130_head
{
this:
np:hasAssertion
dgn-np:NP207177.RALB-Za9DfRE4_5k4PCE3KfEW40BCZrrQbYKoP8MU7hQ0130_assertion
;
np:hasProvenance
dgn-np:NP207177.RALB-Za9DfRE4_5k4PCE3KfEW40BCZrrQbYKoP8MU7hQ0130_provenance
;
np:hasPublicationInfo
dgn-np:NP207177.RALB-Za9DfRE4_5k4PCE3KfEW40BCZrrQbYKoP8MU7hQ0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP207177.RALB-Za9DfRE4_5k4PCE3KfEW40BCZrrQbYKoP8MU7hQ0130_assertion
a
np:Assertion
.
dgn-np:NP207177.RALB-Za9DfRE4_5k4PCE3KfEW40BCZrrQbYKoP8MU7hQ0130_provenance
a
np:Provenance
.
dgn-np:NP207177.RALB-Za9DfRE4_5k4PCE3KfEW40BCZrrQbYKoP8MU7hQ0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP207177.RALB-Za9DfRE4_5k4PCE3KfEW40BCZrrQbYKoP8MU7hQ0130_assertion
{
miriam-gene:595
a
ncit:C16612
.
lld:C0334634
a
ncit:C7057
.
dgn-gda:DGN4b5dd1b888ddc3f70b3cbc678eb42fd4
sio:SIO_000628
miriam-gene:595
,
lld:C0334634
;
a
sio:SIO_001121
.
}
dgn-np:NP207177.RALB-Za9DfRE4_5k4PCE3KfEW40BCZrrQbYKoP8MU7hQ0130_provenance
{
dgn-np:NP207177.RALB-Za9DfRE4_5k4PCE3KfEW40BCZrrQbYKoP8MU7hQ0130_assertion
dcterms:description
"[The predominant expression of a cyclin D1 mRNA isoform lacking the 3'-untranslated region (Delta3'UTR) is associated with higher total cyclin D1 mRNA levels, increased proliferation and poor prognosis in mantle cell lymphoma, and can be caused by genetic alterations of the 3'UTR region.]. 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:17629555
;
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:NP207177.RALB-Za9DfRE4_5k4PCE3KfEW40BCZrrQbYKoP8MU7hQ0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:54+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" .
}