@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP693572.RA1r6k_GoLqWx4jC0vo7cx85n1ZWq5FOml95H237OujT8
> .
@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:NP693572.RA1r6k_GoLqWx4jC0vo7cx85n1ZWq5FOml95H237OujT8130_head
{
this:
np:hasAssertion
dgn-np:NP693572.RA1r6k_GoLqWx4jC0vo7cx85n1ZWq5FOml95H237OujT8130_assertion
;
np:hasProvenance
dgn-np:NP693572.RA1r6k_GoLqWx4jC0vo7cx85n1ZWq5FOml95H237OujT8130_provenance
;
np:hasPublicationInfo
dgn-np:NP693572.RA1r6k_GoLqWx4jC0vo7cx85n1ZWq5FOml95H237OujT8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP693572.RA1r6k_GoLqWx4jC0vo7cx85n1ZWq5FOml95H237OujT8130_assertion
a
np:Assertion
.
dgn-np:NP693572.RA1r6k_GoLqWx4jC0vo7cx85n1ZWq5FOml95H237OujT8130_provenance
a
np:Provenance
.
dgn-np:NP693572.RA1r6k_GoLqWx4jC0vo7cx85n1ZWq5FOml95H237OujT8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP693572.RA1r6k_GoLqWx4jC0vo7cx85n1ZWq5FOml95H237OujT8130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0024266
a
ncit:C7057
.
dgn-gda:DGN538ed89c5ee1fee45015648621eb9d0d
sio:SIO_000628
miriam-gene:7157
,
lld:C0024266
;
a
sio:SIO_001121
.
}
dgn-np:NP693572.RA1r6k_GoLqWx4jC0vo7cx85n1ZWq5FOml95H237OujT8130_provenance
{
dgn-np:NP693572.RA1r6k_GoLqWx4jC0vo7cx85n1ZWq5FOml95H237OujT8130_assertion
dcterms:description
"[The purpose of this study was to assess more accurately the incidence and types of p53 mutations in Barrett's esophagus (BE) with and without dysplasia and in esophageal adenocarcinoma, using pure preparations of epithelial cells obtained by laser capture microdissection (LCM).]. 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:15257314
;
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:NP693572.RA1r6k_GoLqWx4jC0vo7cx85n1ZWq5FOml95H237OujT8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:01+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" .
}