@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP884393.RACVEvEnnu2niV7713SaeNR5W8z2Ia_P8xnGqizVV65Co
> .
@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:NP884393.RACVEvEnnu2niV7713SaeNR5W8z2Ia_P8xnGqizVV65Co130_head
{
this:
np:hasAssertion
dgn-np:NP884393.RACVEvEnnu2niV7713SaeNR5W8z2Ia_P8xnGqizVV65Co130_assertion
;
np:hasProvenance
dgn-np:NP884393.RACVEvEnnu2niV7713SaeNR5W8z2Ia_P8xnGqizVV65Co130_provenance
;
np:hasPublicationInfo
dgn-np:NP884393.RACVEvEnnu2niV7713SaeNR5W8z2Ia_P8xnGqizVV65Co130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP884393.RACVEvEnnu2niV7713SaeNR5W8z2Ia_P8xnGqizVV65Co130_assertion
a
np:Assertion
.
dgn-np:NP884393.RACVEvEnnu2niV7713SaeNR5W8z2Ia_P8xnGqizVV65Co130_provenance
a
np:Provenance
.
dgn-np:NP884393.RACVEvEnnu2niV7713SaeNR5W8z2Ia_P8xnGqizVV65Co130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP884393.RACVEvEnnu2niV7713SaeNR5W8z2Ia_P8xnGqizVV65Co130_assertion
{
miriam-gene:26871
a
ncit:C16612
.
lld:C1970209
a
ncit:C7057
.
dgn-gda:DGNd76bcc4b012a694fc057ba63e3b8813b
sio:SIO_000628
miriam-gene:26871
,
lld:C1970209
;
a
sio:SIO_001121
.
}
dgn-np:NP884393.RACVEvEnnu2niV7713SaeNR5W8z2Ia_P8xnGqizVV65Co130_provenance
{
dgn-np:NP884393.RACVEvEnnu2niV7713SaeNR5W8z2Ia_P8xnGqizVV65Co130_assertion
dcterms:description
"[Adenovirus type 12 (Ad12) infection of human cells induces four chromosomal fragile sites corresponding to the U1 small nuclear RNA (snRNA) genes (the RNU1 locus), the U2 snRNA genes (RNU2), the U1 snRNA pseudogenes (PSU1), and the 5S rRNA genes (RN5S).]. 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:9557707
;
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:NP884393.RACVEvEnnu2niV7713SaeNR5W8z2Ia_P8xnGqizVV65Co130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:38+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" .
}