@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP518531.RASy9q61B_ERZVOwgqoZzhs2ijLOReq1LBGCsiO4l5ZOM
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP518531.RASy9q61B_ERZVOwgqoZzhs2ijLOReq1LBGCsiO4l5ZOM130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP518531.RASy9q61B_ERZVOwgqoZzhs2ijLOReq1LBGCsiO4l5ZOM130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP518531.RASy9q61B_ERZVOwgqoZzhs2ijLOReq1LBGCsiO4l5ZOM130_assertion
a
np:Assertion
.
dgn-np:NP518531.RASy9q61B_ERZVOwgqoZzhs2ijLOReq1LBGCsiO4l5ZOM130_provenance
a
np:Provenance
.
dgn-np:NP518531.RASy9q61B_ERZVOwgqoZzhs2ijLOReq1LBGCsiO4l5ZOM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP518531.RASy9q61B_ERZVOwgqoZzhs2ijLOReq1LBGCsiO4l5ZOM130_assertion
{
miriam-gene:8170
a
ncit:C16612
.
lld:C0334634
a
ncit:C7057
.
dgn-gda:DGN9ba0f055e404c0efe54338690be351b7
sio:SIO_000628
miriam-gene:8170
,
lld:C0334634
;
a
sio:SIO_001121
.
}
dgn-np:NP518531.RASy9q61B_ERZVOwgqoZzhs2ijLOReq1LBGCsiO4l5ZOM130_provenance
{
dgn-np:NP518531.RASy9q61B_ERZVOwgqoZzhs2ijLOReq1LBGCsiO4l5ZOM130_assertion
dcterms:description
"[Taken together, our data highlight the regulatory role of the cyclin D1 3'UTR in the expression and phenotype of cyclin D1 and suggest that in MCL and solid tumors with cyclin D1 3'UTR mutations, the loss of microRNA target sites, rather than ARE elements contribute to the pathogenic overexpression of the cyclin D1 protein.]. 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:19823025
;
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:NP518531.RASy9q61B_ERZVOwgqoZzhs2ijLOReq1LBGCsiO4l5ZOM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:08+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
<
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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
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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