@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP938539.RAJ5ZQoKhGk4hD-EIjEP2y1IqCjzfB8XLIJ1UHzFDglWM
> .
@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:NP938539.RAJ5ZQoKhGk4hD-EIjEP2y1IqCjzfB8XLIJ1UHzFDglWM130_head
{
this:
np:hasAssertion
dgn-np:NP938539.RAJ5ZQoKhGk4hD-EIjEP2y1IqCjzfB8XLIJ1UHzFDglWM130_assertion
;
np:hasProvenance
dgn-np:NP938539.RAJ5ZQoKhGk4hD-EIjEP2y1IqCjzfB8XLIJ1UHzFDglWM130_provenance
;
np:hasPublicationInfo
dgn-np:NP938539.RAJ5ZQoKhGk4hD-EIjEP2y1IqCjzfB8XLIJ1UHzFDglWM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP938539.RAJ5ZQoKhGk4hD-EIjEP2y1IqCjzfB8XLIJ1UHzFDglWM130_assertion
a
np:Assertion
.
dgn-np:NP938539.RAJ5ZQoKhGk4hD-EIjEP2y1IqCjzfB8XLIJ1UHzFDglWM130_provenance
a
np:Provenance
.
dgn-np:NP938539.RAJ5ZQoKhGk4hD-EIjEP2y1IqCjzfB8XLIJ1UHzFDglWM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP938539.RAJ5ZQoKhGk4hD-EIjEP2y1IqCjzfB8XLIJ1UHzFDglWM130_assertion
{
miriam-gene:2272
a
ncit:C16612
.
lld:C0149678
a
ncit:C7057
.
dgn-gda:DGNe9c5a8300dd945d2495164d1daa0432b
sio:SIO_000628
miriam-gene:2272
,
lld:C0149678
;
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.
}
dgn-np:NP938539.RAJ5ZQoKhGk4hD-EIjEP2y1IqCjzfB8XLIJ1UHzFDglWM130_provenance
{
dgn-np:NP938539.RAJ5ZQoKhGk4hD-EIjEP2y1IqCjzfB8XLIJ1UHzFDglWM130_assertion
dcterms:description
"[In this study, we aimed to precisely define the patterns of allelic loss at the FRA3B site in endemic nasopharyngeal carcinoma and to determine whether an association exists between allelic loss, clinicopathological features and Epstein-Barr virus infection.]. 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:17359554
;
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:NP938539.RAJ5ZQoKhGk4hD-EIjEP2y1IqCjzfB8XLIJ1UHzFDglWM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:35+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" .
}