@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP786677.RAW4vdsNkuIJ5aeKmvu_hTn97JbHUAKOm7FbmXtBb6nOg
> .
@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:NP786677.RAW4vdsNkuIJ5aeKmvu_hTn97JbHUAKOm7FbmXtBb6nOg130_head
{
this:
np:hasAssertion
dgn-np:NP786677.RAW4vdsNkuIJ5aeKmvu_hTn97JbHUAKOm7FbmXtBb6nOg130_assertion
;
np:hasProvenance
dgn-np:NP786677.RAW4vdsNkuIJ5aeKmvu_hTn97JbHUAKOm7FbmXtBb6nOg130_provenance
;
np:hasPublicationInfo
dgn-np:NP786677.RAW4vdsNkuIJ5aeKmvu_hTn97JbHUAKOm7FbmXtBb6nOg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP786677.RAW4vdsNkuIJ5aeKmvu_hTn97JbHUAKOm7FbmXtBb6nOg130_assertion
a
np:Assertion
.
dgn-np:NP786677.RAW4vdsNkuIJ5aeKmvu_hTn97JbHUAKOm7FbmXtBb6nOg130_provenance
a
np:Provenance
.
dgn-np:NP786677.RAW4vdsNkuIJ5aeKmvu_hTn97JbHUAKOm7FbmXtBb6nOg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP786677.RAW4vdsNkuIJ5aeKmvu_hTn97JbHUAKOm7FbmXtBb6nOg130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0349560
a
ncit:C7057
.
dgn-gda:DGN243e47738d82c817a790b664bc2622c6
sio:SIO_000628
miriam-gene:1029
,
lld:C0349560
;
a
sio:SIO_001121
.
}
dgn-np:NP786677.RAW4vdsNkuIJ5aeKmvu_hTn97JbHUAKOm7FbmXtBb6nOg130_provenance
{
dgn-np:NP786677.RAW4vdsNkuIJ5aeKmvu_hTn97JbHUAKOm7FbmXtBb6nOg130_assertion
dcterms:description
"[Co-incident methylation, accompanied by loss of expression, of sigma and p16INK4a was commonly detected in both SCC and VIN III, suggesting that epigenetic silencing of these two genes is an early and important event in vulval neoplasia.]. 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:11896620
;
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:NP786677.RAW4vdsNkuIJ5aeKmvu_hTn97JbHUAKOm7FbmXtBb6nOg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:56+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" .
}