@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP369778.RAOYAWjRl4hbEgCPFfrkuYyC61uG_0uxEcR6HsU-Jjok4
> .
@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:NP369778.RAOYAWjRl4hbEgCPFfrkuYyC61uG_0uxEcR6HsU-Jjok4130_head
{
this:
np:hasAssertion
dgn-np:NP369778.RAOYAWjRl4hbEgCPFfrkuYyC61uG_0uxEcR6HsU-Jjok4130_assertion
;
np:hasProvenance
dgn-np:NP369778.RAOYAWjRl4hbEgCPFfrkuYyC61uG_0uxEcR6HsU-Jjok4130_provenance
;
np:hasPublicationInfo
dgn-np:NP369778.RAOYAWjRl4hbEgCPFfrkuYyC61uG_0uxEcR6HsU-Jjok4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP369778.RAOYAWjRl4hbEgCPFfrkuYyC61uG_0uxEcR6HsU-Jjok4130_assertion
a
np:Assertion
.
dgn-np:NP369778.RAOYAWjRl4hbEgCPFfrkuYyC61uG_0uxEcR6HsU-Jjok4130_provenance
a
np:Provenance
.
dgn-np:NP369778.RAOYAWjRl4hbEgCPFfrkuYyC61uG_0uxEcR6HsU-Jjok4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP369778.RAOYAWjRl4hbEgCPFfrkuYyC61uG_0uxEcR6HsU-Jjok4130_assertion
{
miriam-gene:118429
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGN070f83cf342c6a464e2fcb6ebfd3bfd2
sio:SIO_000628
miriam-gene:118429
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP369778.RAOYAWjRl4hbEgCPFfrkuYyC61uG_0uxEcR6HsU-Jjok4130_provenance
{
dgn-np:NP369778.RAOYAWjRl4hbEgCPFfrkuYyC61uG_0uxEcR6HsU-Jjok4130_assertion
dcterms:description
"[To elucidate these associations, we investigated the presence of EBV in 142 cases of esophageal carcinoma, 107 cases of ampulla of Vater carcinoma, and 274 cases of colorectal carcinoma in Korean patients using EBV-encoded small RNAs (EBER)-in situ hybridization (ISH).]. 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:11274639
;
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:NP369778.RAOYAWjRl4hbEgCPFfrkuYyC61uG_0uxEcR6HsU-Jjok4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:36+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
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"v2.1.0" .
}