@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP370768.RA7wYH4OgIwjzDJkP2bDogitNrKiKyCJHPLBONwOR_ar0
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP370768.RA7wYH4OgIwjzDJkP2bDogitNrKiKyCJHPLBONwOR_ar0130_head
{
this:
np:hasAssertion
dgn-np:NP370768.RA7wYH4OgIwjzDJkP2bDogitNrKiKyCJHPLBONwOR_ar0130_assertion
;
np:hasProvenance
dgn-np:NP370768.RA7wYH4OgIwjzDJkP2bDogitNrKiKyCJHPLBONwOR_ar0130_provenance
;
np:hasPublicationInfo
dgn-np:NP370768.RA7wYH4OgIwjzDJkP2bDogitNrKiKyCJHPLBONwOR_ar0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP370768.RA7wYH4OgIwjzDJkP2bDogitNrKiKyCJHPLBONwOR_ar0130_assertion
a
np:Assertion
.
dgn-np:NP370768.RA7wYH4OgIwjzDJkP2bDogitNrKiKyCJHPLBONwOR_ar0130_provenance
a
np:Provenance
.
dgn-np:NP370768.RA7wYH4OgIwjzDJkP2bDogitNrKiKyCJHPLBONwOR_ar0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP370768.RA7wYH4OgIwjzDJkP2bDogitNrKiKyCJHPLBONwOR_ar0130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0279626
a
ncit:C7057
.
dgn-gda:DGN7c37e8ff7704e4024b7a606098c32d4f
sio:SIO_000628
miriam-gene:1029
,
lld:C0279626
;
a
sio:SIO_001121
.
}
dgn-np:NP370768.RA7wYH4OgIwjzDJkP2bDogitNrKiKyCJHPLBONwOR_ar0130_provenance
{
dgn-np:NP370768.RA7wYH4OgIwjzDJkP2bDogitNrKiKyCJHPLBONwOR_ar0130_assertion
dcterms:description
"[Our results suggest that hypermethylation of key genes, such as p16(INK4a), p14(ARF) and hMLH1, may be used in combination with other molecular changes, such as p53 mutation, in the development of biomarkers for predicting the risk for ESCC.]. 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:12376481
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP370768.RA7wYH4OgIwjzDJkP2bDogitNrKiKyCJHPLBONwOR_ar0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:33+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}