@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP990532.RAe9njxqfZF7xCu-Ld8Rm-JtIVwnEMZgZ_I5CCeE_FMnc
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP990532.RAe9njxqfZF7xCu-Ld8Rm-JtIVwnEMZgZ_I5CCeE_FMnc130_head
{
this:
np:hasAssertion
dgn-np:NP990532.RAe9njxqfZF7xCu-Ld8Rm-JtIVwnEMZgZ_I5CCeE_FMnc130_assertion
;
np:hasProvenance
dgn-np:NP990532.RAe9njxqfZF7xCu-Ld8Rm-JtIVwnEMZgZ_I5CCeE_FMnc130_provenance
;
np:hasPublicationInfo
dgn-np:NP990532.RAe9njxqfZF7xCu-Ld8Rm-JtIVwnEMZgZ_I5CCeE_FMnc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP990532.RAe9njxqfZF7xCu-Ld8Rm-JtIVwnEMZgZ_I5CCeE_FMnc130_assertion
a
np:Assertion
.
dgn-np:NP990532.RAe9njxqfZF7xCu-Ld8Rm-JtIVwnEMZgZ_I5CCeE_FMnc130_provenance
a
np:Provenance
.
dgn-np:NP990532.RAe9njxqfZF7xCu-Ld8Rm-JtIVwnEMZgZ_I5CCeE_FMnc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP990532.RAe9njxqfZF7xCu-Ld8Rm-JtIVwnEMZgZ_I5CCeE_FMnc130_assertion
{
miriam-gene:389421
a
ncit:C16612
.
lld:C1306459
a
ncit:C7057
.
dgn-gda:DGNc389da2fe384b0ecb9ec84e48bd02982
sio:SIO_000628
miriam-gene:389421
,
lld:C1306459
;
a
sio:SIO_001121
.
}
dgn-np:NP990532.RAe9njxqfZF7xCu-Ld8Rm-JtIVwnEMZgZ_I5CCeE_FMnc130_provenance
{
dgn-np:NP990532.RAe9njxqfZF7xCu-Ld8Rm-JtIVwnEMZgZ_I5CCeE_FMnc130_assertion
dcterms:description
"[Our finding that Rpl22 inactivation promotes transformation by inducing expression of Lin28B provides the first insight into the mechanistic basis by which mutations in Rpl22, and perhaps some other RP genes, increases cancer risk.]. 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:22976955
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP990532.RAe9njxqfZF7xCu-Ld8Rm-JtIVwnEMZgZ_I5CCeE_FMnc130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:48+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}