@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP149067.RARTqJFk8w_WOFvFdv91W9UPct82OB0sUCVAixk0HX0X0
> .
@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:NP149067.RARTqJFk8w_WOFvFdv91W9UPct82OB0sUCVAixk0HX0X0130_head
{
this:
np:hasAssertion
dgn-np:NP149067.RARTqJFk8w_WOFvFdv91W9UPct82OB0sUCVAixk0HX0X0130_assertion
;
np:hasProvenance
dgn-np:NP149067.RARTqJFk8w_WOFvFdv91W9UPct82OB0sUCVAixk0HX0X0130_provenance
;
np:hasPublicationInfo
dgn-np:NP149067.RARTqJFk8w_WOFvFdv91W9UPct82OB0sUCVAixk0HX0X0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP149067.RARTqJFk8w_WOFvFdv91W9UPct82OB0sUCVAixk0HX0X0130_assertion
a
np:Assertion
.
dgn-np:NP149067.RARTqJFk8w_WOFvFdv91W9UPct82OB0sUCVAixk0HX0X0130_provenance
a
np:Provenance
.
dgn-np:NP149067.RARTqJFk8w_WOFvFdv91W9UPct82OB0sUCVAixk0HX0X0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP149067.RARTqJFk8w_WOFvFdv91W9UPct82OB0sUCVAixk0HX0X0130_assertion
{
miriam-gene:1880
a
ncit:C16612
.
lld:C0149678
a
ncit:C7057
.
dgn-gda:DGN043a9650c0744c109a96fe29f985468c
sio:SIO_000628
miriam-gene:1880
,
lld:C0149678
;
a
sio:SIO_001123
.
}
dgn-np:NP149067.RARTqJFk8w_WOFvFdv91W9UPct82OB0sUCVAixk0HX0X0130_provenance
{
dgn-np:NP149067.RARTqJFk8w_WOFvFdv91W9UPct82OB0sUCVAixk0HX0X0130_assertion
dcterms:description
"[Based on the constitutive signaling and cellular expression pattern of EBI2, it is suggested that it may function in conjunction with BILF1 in the reprogramming of the cell during EBV 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:16540462
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP149067.RARTqJFk8w_WOFvFdv91W9UPct82OB0sUCVAixk0HX0X0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:19+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" .
}