@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP667306.RAHpD7gkI1EZlAAGAEQbBmy6bPzvjmOkwoDaJAKOMsicc
> .
@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:NP667306.RAHpD7gkI1EZlAAGAEQbBmy6bPzvjmOkwoDaJAKOMsicc130_head
{
this:
np:hasAssertion
dgn-np:NP667306.RAHpD7gkI1EZlAAGAEQbBmy6bPzvjmOkwoDaJAKOMsicc130_assertion
;
np:hasProvenance
dgn-np:NP667306.RAHpD7gkI1EZlAAGAEQbBmy6bPzvjmOkwoDaJAKOMsicc130_provenance
;
np:hasPublicationInfo
dgn-np:NP667306.RAHpD7gkI1EZlAAGAEQbBmy6bPzvjmOkwoDaJAKOMsicc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP667306.RAHpD7gkI1EZlAAGAEQbBmy6bPzvjmOkwoDaJAKOMsicc130_assertion
a
np:Assertion
.
dgn-np:NP667306.RAHpD7gkI1EZlAAGAEQbBmy6bPzvjmOkwoDaJAKOMsicc130_provenance
a
np:Provenance
.
dgn-np:NP667306.RAHpD7gkI1EZlAAGAEQbBmy6bPzvjmOkwoDaJAKOMsicc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP667306.RAHpD7gkI1EZlAAGAEQbBmy6bPzvjmOkwoDaJAKOMsicc130_assertion
{
miriam-gene:1612
a
ncit:C16612
.
lld:C0014859
a
ncit:C7057
.
dgn-gda:DGN5e41c1b9b1815b8e30d340a923b3c6c0
sio:SIO_000628
miriam-gene:1612
,
lld:C0014859
;
a
sio:SIO_001121
.
}
dgn-np:NP667306.RAHpD7gkI1EZlAAGAEQbBmy6bPzvjmOkwoDaJAKOMsicc130_provenance
{
dgn-np:NP667306.RAHpD7gkI1EZlAAGAEQbBmy6bPzvjmOkwoDaJAKOMsicc130_assertion
dcterms:description
"[Thirty-six of 59 patients (61.0%) with esophageal cancer had detectable levels of methylated DAPK or APC promoter DNA and preoperative detection was significantly associated with an unfavorable prognosis as revealed by multivariate Cox proportional hazards regression analysis [Exp(b) = 4.578; P = 0.01].]. 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:19259700
;
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:NP667306.RAHpD7gkI1EZlAAGAEQbBmy6bPzvjmOkwoDaJAKOMsicc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:43+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" .
}