@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP248590.RAbylKnM-sSECLBOF8Veg-Kb456A-B9febE8gSyZxl8IU
> .
@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:NP248590.RAbylKnM-sSECLBOF8Veg-Kb456A-B9febE8gSyZxl8IU130_head
{
this:
np:hasAssertion
dgn-np:NP248590.RAbylKnM-sSECLBOF8Veg-Kb456A-B9febE8gSyZxl8IU130_assertion
;
np:hasProvenance
dgn-np:NP248590.RAbylKnM-sSECLBOF8Veg-Kb456A-B9febE8gSyZxl8IU130_provenance
;
np:hasPublicationInfo
dgn-np:NP248590.RAbylKnM-sSECLBOF8Veg-Kb456A-B9febE8gSyZxl8IU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP248590.RAbylKnM-sSECLBOF8Veg-Kb456A-B9febE8gSyZxl8IU130_assertion
a
np:Assertion
.
dgn-np:NP248590.RAbylKnM-sSECLBOF8Veg-Kb456A-B9febE8gSyZxl8IU130_provenance
a
np:Provenance
.
dgn-np:NP248590.RAbylKnM-sSECLBOF8Veg-Kb456A-B9febE8gSyZxl8IU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP248590.RAbylKnM-sSECLBOF8Veg-Kb456A-B9febE8gSyZxl8IU130_assertion
{
miriam-gene:3081
a
ncit:C16612
.
lld:C0279628
a
ncit:C7057
.
dgn-gda:DGN93f7c14d61a8c80acecd7a0cc81d3bbc
sio:SIO_000628
miriam-gene:3081
,
lld:C0279628
;
a
sio:SIO_001121
.
}
dgn-np:NP248590.RAbylKnM-sSECLBOF8Veg-Kb456A-B9febE8gSyZxl8IU130_provenance
{
dgn-np:NP248590.RAbylKnM-sSECLBOF8Veg-Kb456A-B9febE8gSyZxl8IU130_assertion
dcterms:description
"[These findings suggest that FISH has high sensitivity for the detection of dysplasia and EA in BE patients, with the power to stratify patients by FISH abnormality for progression to HGD/EA.]. 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:18602665
;
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:NP248590.RAbylKnM-sSECLBOF8Veg-Kb456A-B9febE8gSyZxl8IU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:19+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" .
}