@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP158928.RA9uOb2mP2_WDj00C1j6MiGoEcB90WH-qK3GnCevrOPtE
> .
@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:NP158928.RA9uOb2mP2_WDj00C1j6MiGoEcB90WH-qK3GnCevrOPtE130_head
{
this:
np:hasAssertion
dgn-np:NP158928.RA9uOb2mP2_WDj00C1j6MiGoEcB90WH-qK3GnCevrOPtE130_assertion
;
np:hasProvenance
dgn-np:NP158928.RA9uOb2mP2_WDj00C1j6MiGoEcB90WH-qK3GnCevrOPtE130_provenance
;
np:hasPublicationInfo
dgn-np:NP158928.RA9uOb2mP2_WDj00C1j6MiGoEcB90WH-qK3GnCevrOPtE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP158928.RA9uOb2mP2_WDj00C1j6MiGoEcB90WH-qK3GnCevrOPtE130_assertion
a
np:Assertion
.
dgn-np:NP158928.RA9uOb2mP2_WDj00C1j6MiGoEcB90WH-qK3GnCevrOPtE130_provenance
a
np:Provenance
.
dgn-np:NP158928.RA9uOb2mP2_WDj00C1j6MiGoEcB90WH-qK3GnCevrOPtE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP158928.RA9uOb2mP2_WDj00C1j6MiGoEcB90WH-qK3GnCevrOPtE130_assertion
{
miriam-gene:595
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNaf36c78305efcf11671cd9f912450383
sio:SIO_000628
miriam-gene:595
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP158928.RA9uOb2mP2_WDj00C1j6MiGoEcB90WH-qK3GnCevrOPtE130_provenance
{
dgn-np:NP158928.RA9uOb2mP2_WDj00C1j6MiGoEcB90WH-qK3GnCevrOPtE130_assertion
dcterms:description
"[To date, biomarkers which currently appear to predict the progression of Barrett esophagus to invasive malignancy include aneuploidy, loss of heterozygosity of 17p (implicating the p53 tumor suppressor gene), and cyclin D1 protein overexpression, and with further validation, will most likely be incorporated into routine clinical practice.]. 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:16428034
;
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:NP158928.RA9uOb2mP2_WDj00C1j6MiGoEcB90WH-qK3GnCevrOPtE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:25+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" .
}