@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP616399.RA6X6dbaGK_nsP9OGt0CFQgZO6njpl22LDreVMEYghwak
> .
@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:NP616399.RA6X6dbaGK_nsP9OGt0CFQgZO6njpl22LDreVMEYghwak130_head
{
this:
np:hasAssertion
dgn-np:NP616399.RA6X6dbaGK_nsP9OGt0CFQgZO6njpl22LDreVMEYghwak130_assertion
;
np:hasProvenance
dgn-np:NP616399.RA6X6dbaGK_nsP9OGt0CFQgZO6njpl22LDreVMEYghwak130_provenance
;
np:hasPublicationInfo
dgn-np:NP616399.RA6X6dbaGK_nsP9OGt0CFQgZO6njpl22LDreVMEYghwak130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP616399.RA6X6dbaGK_nsP9OGt0CFQgZO6njpl22LDreVMEYghwak130_assertion
a
np:Assertion
.
dgn-np:NP616399.RA6X6dbaGK_nsP9OGt0CFQgZO6njpl22LDreVMEYghwak130_provenance
a
np:Provenance
.
dgn-np:NP616399.RA6X6dbaGK_nsP9OGt0CFQgZO6njpl22LDreVMEYghwak130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP616399.RA6X6dbaGK_nsP9OGt0CFQgZO6njpl22LDreVMEYghwak130_assertion
{
miriam-gene:6469
a
ncit:C16612
.
lld:C2931822
a
ncit:C7057
.
dgn-gda:DGN08b6599180315aa2fa52f58038230ad3
sio:SIO_000628
miriam-gene:6469
,
lld:C2931822
;
a
sio:SIO_001121
.
}
dgn-np:NP616399.RA6X6dbaGK_nsP9OGt0CFQgZO6njpl22LDreVMEYghwak130_provenance
{
dgn-np:NP616399.RA6X6dbaGK_nsP9OGt0CFQgZO6njpl22LDreVMEYghwak130_assertion
dcterms:description
"[Using authentic EBV-positive carcinoma-derived cell lines and nasopharyngeal epithelial cell lines latently infected with EBV as models for NPC in vitro, we show that EBV activates the HH signalling pathway through autocrine induction of SHH ligand.]. 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:23934731
;
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:NP616399.RA6X6dbaGK_nsP9OGt0CFQgZO6njpl22LDreVMEYghwak130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:12+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" .
}