@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP553292.RAAfHgLCfR3X3AB7IdMGHqoonYIAcDfCobDd5tWW5RkN4
> .
@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:NP553292.RAAfHgLCfR3X3AB7IdMGHqoonYIAcDfCobDd5tWW5RkN4130_head
{
this:
np:hasAssertion
dgn-np:NP553292.RAAfHgLCfR3X3AB7IdMGHqoonYIAcDfCobDd5tWW5RkN4130_assertion
;
np:hasProvenance
dgn-np:NP553292.RAAfHgLCfR3X3AB7IdMGHqoonYIAcDfCobDd5tWW5RkN4130_provenance
;
np:hasPublicationInfo
dgn-np:NP553292.RAAfHgLCfR3X3AB7IdMGHqoonYIAcDfCobDd5tWW5RkN4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP553292.RAAfHgLCfR3X3AB7IdMGHqoonYIAcDfCobDd5tWW5RkN4130_assertion
a
np:Assertion
.
dgn-np:NP553292.RAAfHgLCfR3X3AB7IdMGHqoonYIAcDfCobDd5tWW5RkN4130_provenance
a
np:Provenance
.
dgn-np:NP553292.RAAfHgLCfR3X3AB7IdMGHqoonYIAcDfCobDd5tWW5RkN4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP553292.RAAfHgLCfR3X3AB7IdMGHqoonYIAcDfCobDd5tWW5RkN4130_assertion
{
miriam-gene:5313
a
ncit:C16612
.
lld:C0015625
a
ncit:C7057
.
dgn-gda:DGNbae714a0181bb0688de8100081e828d8
sio:SIO_000628
miriam-gene:5313
,
lld:C0015625
;
a
sio:SIO_001121
.
}
dgn-np:NP553292.RAAfHgLCfR3X3AB7IdMGHqoonYIAcDfCobDd5tWW5RkN4130_provenance
{
dgn-np:NP553292.RAAfHgLCfR3X3AB7IdMGHqoonYIAcDfCobDd5tWW5RkN4130_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:NP553292.RAAfHgLCfR3X3AB7IdMGHqoonYIAcDfCobDd5tWW5RkN4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:33+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" .
}