@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP204662.RAoPp-92PYd3_n6vyfncX9VIigVDXqeLQVj0mZVDV5sTU
> .
@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:NP204662.RAoPp-92PYd3_n6vyfncX9VIigVDXqeLQVj0mZVDV5sTU130_head
{
this:
np:hasAssertion
dgn-np:NP204662.RAoPp-92PYd3_n6vyfncX9VIigVDXqeLQVj0mZVDV5sTU130_assertion
;
np:hasProvenance
dgn-np:NP204662.RAoPp-92PYd3_n6vyfncX9VIigVDXqeLQVj0mZVDV5sTU130_provenance
;
np:hasPublicationInfo
dgn-np:NP204662.RAoPp-92PYd3_n6vyfncX9VIigVDXqeLQVj0mZVDV5sTU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP204662.RAoPp-92PYd3_n6vyfncX9VIigVDXqeLQVj0mZVDV5sTU130_assertion
a
np:Assertion
.
dgn-np:NP204662.RAoPp-92PYd3_n6vyfncX9VIigVDXqeLQVj0mZVDV5sTU130_provenance
a
np:Provenance
.
dgn-np:NP204662.RAoPp-92PYd3_n6vyfncX9VIigVDXqeLQVj0mZVDV5sTU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP204662.RAoPp-92PYd3_n6vyfncX9VIigVDXqeLQVj0mZVDV5sTU130_assertion
{
miriam-gene:2272
a
ncit:C16612
.
lld:C0032927
a
ncit:C7057
.
dgn-gda:DGN0d71704579418aff6246551b50331aae
sio:SIO_000628
miriam-gene:2272
,
lld:C0032927
;
a
sio:SIO_001121
.
}
dgn-np:NP204662.RAoPp-92PYd3_n6vyfncX9VIigVDXqeLQVj0mZVDV5sTU130_provenance
{
dgn-np:NP204662.RAoPp-92PYd3_n6vyfncX9VIigVDXqeLQVj0mZVDV5sTU130_assertion
dcterms:description
"[The purpose of this study was to investigate aberrant promoter methylation of the p16 and FHIT genes in tissues and plasma and loss of protein expression in esophageal precancerous conditions (EPC) and esophageal squamous cell carcinoma (ESCC) of high-risk area.]. 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:18365557
;
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:NP204662.RAoPp-92PYd3_n6vyfncX9VIigVDXqeLQVj0mZVDV5sTU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:53+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" .
}