@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP546472.RAOAi8b2TiQZofralsl4A4KrzoC5Eu-Fyc-A55hj78-es
> .
@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:NP546472.RAOAi8b2TiQZofralsl4A4KrzoC5Eu-Fyc-A55hj78-es130_head
{
this:
np:hasAssertion
dgn-np:NP546472.RAOAi8b2TiQZofralsl4A4KrzoC5Eu-Fyc-A55hj78-es130_assertion
;
np:hasProvenance
dgn-np:NP546472.RAOAi8b2TiQZofralsl4A4KrzoC5Eu-Fyc-A55hj78-es130_provenance
;
np:hasPublicationInfo
dgn-np:NP546472.RAOAi8b2TiQZofralsl4A4KrzoC5Eu-Fyc-A55hj78-es130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP546472.RAOAi8b2TiQZofralsl4A4KrzoC5Eu-Fyc-A55hj78-es130_assertion
a
np:Assertion
.
dgn-np:NP546472.RAOAi8b2TiQZofralsl4A4KrzoC5Eu-Fyc-A55hj78-es130_provenance
a
np:Provenance
.
dgn-np:NP546472.RAOAi8b2TiQZofralsl4A4KrzoC5Eu-Fyc-A55hj78-es130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP546472.RAOAi8b2TiQZofralsl4A4KrzoC5Eu-Fyc-A55hj78-es130_assertion
{
miriam-gene:2968
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNbbd2192a52c61485ef06798b8463d1a9
sio:SIO_000628
miriam-gene:2968
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP546472.RAOAi8b2TiQZofralsl4A4KrzoC5Eu-Fyc-A55hj78-es130_provenance
{
dgn-np:NP546472.RAOAi8b2TiQZofralsl4A4KrzoC5Eu-Fyc-A55hj78-es130_assertion
dcterms:description
"[Together with the role of 19S subunits in transcriptional regulation, homology between S12 and eIF3 and TFIIH subunits, coelution with immunoproteasome subunits, and differential posttranslational modification and nuclear localization, these data suggest a differential nuclear function of modified and unmodified S12 in cancer.]. 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:15221960
;
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:NP546472.RAOAi8b2TiQZofralsl4A4KrzoC5Eu-Fyc-A55hj78-es130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:29+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" .
}