@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP899166.RALnb6CavW3zAsuJdzWNHR9unUjlCdFbWjS7I2-8ByfXQ
> .
@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:NP899166.RALnb6CavW3zAsuJdzWNHR9unUjlCdFbWjS7I2-8ByfXQ130_head
{
this:
np:hasAssertion
dgn-np:NP899166.RALnb6CavW3zAsuJdzWNHR9unUjlCdFbWjS7I2-8ByfXQ130_assertion
;
np:hasProvenance
dgn-np:NP899166.RALnb6CavW3zAsuJdzWNHR9unUjlCdFbWjS7I2-8ByfXQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP899166.RALnb6CavW3zAsuJdzWNHR9unUjlCdFbWjS7I2-8ByfXQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP899166.RALnb6CavW3zAsuJdzWNHR9unUjlCdFbWjS7I2-8ByfXQ130_assertion
a
np:Assertion
.
dgn-np:NP899166.RALnb6CavW3zAsuJdzWNHR9unUjlCdFbWjS7I2-8ByfXQ130_provenance
a
np:Provenance
.
dgn-np:NP899166.RALnb6CavW3zAsuJdzWNHR9unUjlCdFbWjS7I2-8ByfXQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP899166.RALnb6CavW3zAsuJdzWNHR9unUjlCdFbWjS7I2-8ByfXQ130_assertion
{
miriam-gene:5915
a
ncit:C16612
.
lld:C0600139
a
ncit:C7057
.
dgn-gda:DGN2036dc2816c359f1c79a3db6a405dd1e
sio:SIO_000628
miriam-gene:5915
,
lld:C0600139
;
a
sio:SIO_001121
.
}
dgn-np:NP899166.RALnb6CavW3zAsuJdzWNHR9unUjlCdFbWjS7I2-8ByfXQ130_provenance
{
dgn-np:NP899166.RALnb6CavW3zAsuJdzWNHR9unUjlCdFbWjS7I2-8ByfXQ130_assertion
dcterms:description
"[The aim of our study was to evaluate the diagnostic value of aberrant promoter hypermethylation of retinoic acid receptor β2 (RARβ2) gene in serum DNA samples from patients with the diagnosis of PCa and benign prostatic hyperplasia (BPH), as a new epigenetic biomarker in distinguishing between malignant and non-malignant lesions.]. 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:23294958
;
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:NP899166.RALnb6CavW3zAsuJdzWNHR9unUjlCdFbWjS7I2-8ByfXQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:12+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" .
}