@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP190788.RAc7gEkC3x908c4Om5DjTlLdDQCLCfjXS1i7x0rNNS-Qk
> .
@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:NP190788.RAc7gEkC3x908c4Om5DjTlLdDQCLCfjXS1i7x0rNNS-Qk130_head
{
this:
np:hasAssertion
dgn-np:NP190788.RAc7gEkC3x908c4Om5DjTlLdDQCLCfjXS1i7x0rNNS-Qk130_assertion
;
np:hasProvenance
dgn-np:NP190788.RAc7gEkC3x908c4Om5DjTlLdDQCLCfjXS1i7x0rNNS-Qk130_provenance
;
np:hasPublicationInfo
dgn-np:NP190788.RAc7gEkC3x908c4Om5DjTlLdDQCLCfjXS1i7x0rNNS-Qk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP190788.RAc7gEkC3x908c4Om5DjTlLdDQCLCfjXS1i7x0rNNS-Qk130_assertion
a
np:Assertion
.
dgn-np:NP190788.RAc7gEkC3x908c4Om5DjTlLdDQCLCfjXS1i7x0rNNS-Qk130_provenance
a
np:Provenance
.
dgn-np:NP190788.RAc7gEkC3x908c4Om5DjTlLdDQCLCfjXS1i7x0rNNS-Qk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP190788.RAc7gEkC3x908c4Om5DjTlLdDQCLCfjXS1i7x0rNNS-Qk130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0032927
a
ncit:C7057
.
dgn-gda:DGN0415356fd108fff5f56a3005c86f980c
sio:SIO_000628
miriam-gene:1029
,
lld:C0032927
;
a
sio:SIO_001121
.
}
dgn-np:NP190788.RAc7gEkC3x908c4Om5DjTlLdDQCLCfjXS1i7x0rNNS-Qk130_provenance
{
dgn-np:NP190788.RAc7gEkC3x908c4Om5DjTlLdDQCLCfjXS1i7x0rNNS-Qk130_assertion
dcterms:description
"[The aim of this study was to characterize the spectrum of p16 alterations in surgically resected esophageal tissues, comprising histologically normal esophageal squamous and gastric epithelia, premalignant Barrett's epithelia, and associated esophageal adenocarcinomas, and to explore associations between p16 mRNA expression and p16 mutations, deletions, promoter hypermethylation, p16 protein expression, and clinico-pathologic features for the same tissues.]. 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:15617840
;
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:NP190788.RAc7gEkC3x908c4Om5DjTlLdDQCLCfjXS1i7x0rNNS-Qk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:45+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" .
}