@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP381277.RAuoIMnv1u6hzfHZUFYFW82RqbjzrOin-CpqOiXOqNte0
> .
@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:NP381277.RAuoIMnv1u6hzfHZUFYFW82RqbjzrOin-CpqOiXOqNte0130_head
{
this:
np:hasAssertion
dgn-np:NP381277.RAuoIMnv1u6hzfHZUFYFW82RqbjzrOin-CpqOiXOqNte0130_assertion
;
np:hasProvenance
dgn-np:NP381277.RAuoIMnv1u6hzfHZUFYFW82RqbjzrOin-CpqOiXOqNte0130_provenance
;
np:hasPublicationInfo
dgn-np:NP381277.RAuoIMnv1u6hzfHZUFYFW82RqbjzrOin-CpqOiXOqNte0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP381277.RAuoIMnv1u6hzfHZUFYFW82RqbjzrOin-CpqOiXOqNte0130_assertion
a
np:Assertion
.
dgn-np:NP381277.RAuoIMnv1u6hzfHZUFYFW82RqbjzrOin-CpqOiXOqNte0130_provenance
a
np:Provenance
.
dgn-np:NP381277.RAuoIMnv1u6hzfHZUFYFW82RqbjzrOin-CpqOiXOqNte0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP381277.RAuoIMnv1u6hzfHZUFYFW82RqbjzrOin-CpqOiXOqNte0130_assertion
{
miriam-gene:2272
a
ncit:C16612
.
lld:C0546837
a
ncit:C7057
.
dgn-gda:DGNbecb244f8f428735432f41cc06a58fdd
sio:SIO_000628
miriam-gene:2272
,
lld:C0546837
;
a
sio:SIO_001121
.
}
dgn-np:NP381277.RAuoIMnv1u6hzfHZUFYFW82RqbjzrOin-CpqOiXOqNte0130_provenance
{
dgn-np:NP381277.RAuoIMnv1u6hzfHZUFYFW82RqbjzrOin-CpqOiXOqNte0130_assertion
dcterms:description
"[We believe that high-grade atypical hyperplasia in esophageal epithelium and deletion of FHIT gene in esophageal cancer and its resected margin are pathological and molecular markers for early diagnosis of esophageal cancer respectively, and the latter may be one of the molecular markers for the resection.]. 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:12903759
;
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:NP381277.RAuoIMnv1u6hzfHZUFYFW82RqbjzrOin-CpqOiXOqNte0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:45+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" .
}