@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP451867.RAEHk-ZnhIr0giyrxn4vlsUFxIYYlhf0Ay6oXZ5-_DoPQ
> .
@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:NP451867.RAEHk-ZnhIr0giyrxn4vlsUFxIYYlhf0Ay6oXZ5-_DoPQ130_head
{
this:
np:hasAssertion
dgn-np:NP451867.RAEHk-ZnhIr0giyrxn4vlsUFxIYYlhf0Ay6oXZ5-_DoPQ130_assertion
;
np:hasProvenance
dgn-np:NP451867.RAEHk-ZnhIr0giyrxn4vlsUFxIYYlhf0Ay6oXZ5-_DoPQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP451867.RAEHk-ZnhIr0giyrxn4vlsUFxIYYlhf0Ay6oXZ5-_DoPQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP451867.RAEHk-ZnhIr0giyrxn4vlsUFxIYYlhf0Ay6oXZ5-_DoPQ130_assertion
a
np:Assertion
.
dgn-np:NP451867.RAEHk-ZnhIr0giyrxn4vlsUFxIYYlhf0Ay6oXZ5-_DoPQ130_provenance
a
np:Provenance
.
dgn-np:NP451867.RAEHk-ZnhIr0giyrxn4vlsUFxIYYlhf0Ay6oXZ5-_DoPQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP451867.RAEHk-ZnhIr0giyrxn4vlsUFxIYYlhf0Ay6oXZ5-_DoPQ130_assertion
{
miriam-gene:5313
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN79943561c2c687ca2c1cee800f265185
sio:SIO_000628
miriam-gene:5313
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP451867.RAEHk-ZnhIr0giyrxn4vlsUFxIYYlhf0Ay6oXZ5-_DoPQ130_provenance
{
dgn-np:NP451867.RAEHk-ZnhIr0giyrxn4vlsUFxIYYlhf0Ay6oXZ5-_DoPQ130_assertion
dcterms:description
"[Inhibition of PKR by NPM may be one mechanism by which neoplastic clones evolve in sporadic malignancies and in neoplastic cells arising in the context of the cancer predisposition syndrome, Fanconi anemia.]. 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:12882984
;
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:NP451867.RAEHk-ZnhIr0giyrxn4vlsUFxIYYlhf0Ay6oXZ5-_DoPQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:29+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" .
}