@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP447012.RANrWXyLEeDSWyRzxwlST_wlmw0hifpFYBbYC6a2gz6sU
> .
@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:NP447012.RANrWXyLEeDSWyRzxwlST_wlmw0hifpFYBbYC6a2gz6sU130_head
{
this:
np:hasAssertion
dgn-np:NP447012.RANrWXyLEeDSWyRzxwlST_wlmw0hifpFYBbYC6a2gz6sU130_assertion
;
np:hasProvenance
dgn-np:NP447012.RANrWXyLEeDSWyRzxwlST_wlmw0hifpFYBbYC6a2gz6sU130_provenance
;
np:hasPublicationInfo
dgn-np:NP447012.RANrWXyLEeDSWyRzxwlST_wlmw0hifpFYBbYC6a2gz6sU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP447012.RANrWXyLEeDSWyRzxwlST_wlmw0hifpFYBbYC6a2gz6sU130_assertion
a
np:Assertion
.
dgn-np:NP447012.RANrWXyLEeDSWyRzxwlST_wlmw0hifpFYBbYC6a2gz6sU130_provenance
a
np:Provenance
.
dgn-np:NP447012.RANrWXyLEeDSWyRzxwlST_wlmw0hifpFYBbYC6a2gz6sU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP447012.RANrWXyLEeDSWyRzxwlST_wlmw0hifpFYBbYC6a2gz6sU130_assertion
{
miriam-gene:51199
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGN6ab1b59647d9e1607889ae574a2f831d
sio:SIO_000628
miriam-gene:51199
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP447012.RANrWXyLEeDSWyRzxwlST_wlmw0hifpFYBbYC6a2gz6sU130_provenance
{
dgn-np:NP447012.RANrWXyLEeDSWyRzxwlST_wlmw0hifpFYBbYC6a2gz6sU130_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:NP447012.RANrWXyLEeDSWyRzxwlST_wlmw0hifpFYBbYC6a2gz6sU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:26+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" .
}