@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP369844.RAYdyyy0DdnIWEb_hglJpdlQS3JHvk2ZbCOjK0flNJXGI
> .
@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:NP369844.RAYdyyy0DdnIWEb_hglJpdlQS3JHvk2ZbCOjK0flNJXGI130_head
{
this:
np:hasAssertion
dgn-np:NP369844.RAYdyyy0DdnIWEb_hglJpdlQS3JHvk2ZbCOjK0flNJXGI130_assertion
;
np:hasProvenance
dgn-np:NP369844.RAYdyyy0DdnIWEb_hglJpdlQS3JHvk2ZbCOjK0flNJXGI130_provenance
;
np:hasPublicationInfo
dgn-np:NP369844.RAYdyyy0DdnIWEb_hglJpdlQS3JHvk2ZbCOjK0flNJXGI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP369844.RAYdyyy0DdnIWEb_hglJpdlQS3JHvk2ZbCOjK0flNJXGI130_assertion
a
np:Assertion
.
dgn-np:NP369844.RAYdyyy0DdnIWEb_hglJpdlQS3JHvk2ZbCOjK0flNJXGI130_provenance
a
np:Provenance
.
dgn-np:NP369844.RAYdyyy0DdnIWEb_hglJpdlQS3JHvk2ZbCOjK0flNJXGI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP369844.RAYdyyy0DdnIWEb_hglJpdlQS3JHvk2ZbCOjK0flNJXGI130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0206708
a
ncit:C7057
.
dgn-gda:DGN691e8a9c38fae1dab37d5091debdac43
sio:SIO_000628
miriam-gene:1029
,
lld:C0206708
;
a
sio:SIO_001121
.
}
dgn-np:NP369844.RAYdyyy0DdnIWEb_hglJpdlQS3JHvk2ZbCOjK0flNJXGI130_provenance
{
dgn-np:NP369844.RAYdyyy0DdnIWEb_hglJpdlQS3JHvk2ZbCOjK0flNJXGI130_assertion
dcterms:description
"[The hypermethylation of p16 INK4A and MGMT genes in the uterine cervix may indicate the presence of malignant cells, and p16 INK4A immunostaining is useful in grading CIN and diagnosing invasive SCC and adenocarcinoma.]. 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:15785933
;
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:NP369844.RAYdyyy0DdnIWEb_hglJpdlQS3JHvk2ZbCOjK0flNJXGI130_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
pav:version
"v2.1.0" .
}