@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP882033.RArYI6swgBXcwaK9Agp582n3VxglbNFrL20_T4nG5Su4k
> .
@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:NP882033.RArYI6swgBXcwaK9Agp582n3VxglbNFrL20_T4nG5Su4k130_head
{
this:
np:hasAssertion
dgn-np:NP882033.RArYI6swgBXcwaK9Agp582n3VxglbNFrL20_T4nG5Su4k130_assertion
;
np:hasProvenance
dgn-np:NP882033.RArYI6swgBXcwaK9Agp582n3VxglbNFrL20_T4nG5Su4k130_provenance
;
np:hasPublicationInfo
dgn-np:NP882033.RArYI6swgBXcwaK9Agp582n3VxglbNFrL20_T4nG5Su4k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP882033.RArYI6swgBXcwaK9Agp582n3VxglbNFrL20_T4nG5Su4k130_assertion
a
np:Assertion
.
dgn-np:NP882033.RArYI6swgBXcwaK9Agp582n3VxglbNFrL20_T4nG5Su4k130_provenance
a
np:Provenance
.
dgn-np:NP882033.RArYI6swgBXcwaK9Agp582n3VxglbNFrL20_T4nG5Su4k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP882033.RArYI6swgBXcwaK9Agp582n3VxglbNFrL20_T4nG5Su4k130_assertion
{
miriam-gene:10428
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNfb1cfc3b25b6a58be1b7918d630df8fb
sio:SIO_000628
miriam-gene:10428
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP882033.RArYI6swgBXcwaK9Agp582n3VxglbNFrL20_T4nG5Su4k130_provenance
{
dgn-np:NP882033.RArYI6swgBXcwaK9Agp582n3VxglbNFrL20_T4nG5Su4k130_assertion
dcterms:description
"[In addition, the levels of the E7 oncoprotein were at least as high as in cancer derived cell lines, suggesting that E2 interruption, observed in cancer derived cell lines, is not causally related to the high level of E7 expression and, therefore, deregulation of the P97 promoter may not be a prerequisite for HPV-16 associated cancer development.]. 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:1651587
;
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:NP882033.RArYI6swgBXcwaK9Agp582n3VxglbNFrL20_T4nG5Su4k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:59+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" .
}