@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP51206.RAYezUrthFahsK_P4XQblyW3xvmKkH-7AurAcMw-g76Is
> .
@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:NP51206.RAYezUrthFahsK_P4XQblyW3xvmKkH-7AurAcMw-g76Is130_head
{
this:
np:hasAssertion
dgn-np:NP51206.RAYezUrthFahsK_P4XQblyW3xvmKkH-7AurAcMw-g76Is130_assertion
;
np:hasProvenance
dgn-np:NP51206.RAYezUrthFahsK_P4XQblyW3xvmKkH-7AurAcMw-g76Is130_provenance
;
np:hasPublicationInfo
dgn-np:NP51206.RAYezUrthFahsK_P4XQblyW3xvmKkH-7AurAcMw-g76Is130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP51206.RAYezUrthFahsK_P4XQblyW3xvmKkH-7AurAcMw-g76Is130_assertion
a
np:Assertion
.
dgn-np:NP51206.RAYezUrthFahsK_P4XQblyW3xvmKkH-7AurAcMw-g76Is130_provenance
a
np:Provenance
.
dgn-np:NP51206.RAYezUrthFahsK_P4XQblyW3xvmKkH-7AurAcMw-g76Is130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP51206.RAYezUrthFahsK_P4XQblyW3xvmKkH-7AurAcMw-g76Is130_assertion
{
miriam-gene:6648
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGNc6ed9e94b06bfa8383e68ff8c8b9b2b3
sio:SIO_000628
miriam-gene:6648
,
lld:C0376358
;
a
sio:SIO_001122
.
}
dgn-np:NP51206.RAYezUrthFahsK_P4XQblyW3xvmKkH-7AurAcMw-g76Is130_provenance
{
dgn-np:NP51206.RAYezUrthFahsK_P4XQblyW3xvmKkH-7AurAcMw-g76Is130_assertion
dcterms:description
"[These data suggest that the relationship between circulating selenium levels at diagnosis and prognostic risk of prostate cancer is modified by SOD2 genotype and indicate caution against broad use of selenium supplementation for men with prostate cancer.]. 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:19528373
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP51206.RAYezUrthFahsK_P4XQblyW3xvmKkH-7AurAcMw-g76Is130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:23+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" .
}