@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP361225.RAmuApcLzHYVDLkcEn5EJgMVJ9xgD_za-PrmdydsE3M5M
> .
@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:NP361225.RAmuApcLzHYVDLkcEn5EJgMVJ9xgD_za-PrmdydsE3M5M130_head
{
this:
np:hasAssertion
dgn-np:NP361225.RAmuApcLzHYVDLkcEn5EJgMVJ9xgD_za-PrmdydsE3M5M130_assertion
;
np:hasProvenance
dgn-np:NP361225.RAmuApcLzHYVDLkcEn5EJgMVJ9xgD_za-PrmdydsE3M5M130_provenance
;
np:hasPublicationInfo
dgn-np:NP361225.RAmuApcLzHYVDLkcEn5EJgMVJ9xgD_za-PrmdydsE3M5M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP361225.RAmuApcLzHYVDLkcEn5EJgMVJ9xgD_za-PrmdydsE3M5M130_assertion
a
np:Assertion
.
dgn-np:NP361225.RAmuApcLzHYVDLkcEn5EJgMVJ9xgD_za-PrmdydsE3M5M130_provenance
a
np:Provenance
.
dgn-np:NP361225.RAmuApcLzHYVDLkcEn5EJgMVJ9xgD_za-PrmdydsE3M5M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP361225.RAmuApcLzHYVDLkcEn5EJgMVJ9xgD_za-PrmdydsE3M5M130_assertion
{
miriam-gene:57026
a
ncit:C16612
.
lld:C1709246
a
ncit:C7057
.
dgn-gda:DGN4adacae74e608ca700ecd5492d5b89d7
sio:SIO_000628
miriam-gene:57026
,
lld:C1709246
;
a
sio:SIO_001121
.
}
dgn-np:NP361225.RAmuApcLzHYVDLkcEn5EJgMVJ9xgD_za-PrmdydsE3M5M130_provenance
{
dgn-np:NP361225.RAmuApcLzHYVDLkcEn5EJgMVJ9xgD_za-PrmdydsE3M5M130_assertion
dcterms:description
"[Chfr and hMLH1 hypermethylation, which may lead to chromosomal instability (CIN) and microsatellite instability (MSI), respectively, was analyzed in gastric noninvasive neoplasias (NIN, Padova international classification) and submucosal invasive adenocarcinomas and in their corresponding non-neoplastic gastric epithelia.]. 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:15735977
;
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:NP361225.RAmuApcLzHYVDLkcEn5EJgMVJ9xgD_za-PrmdydsE3M5M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:31+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" .
}