@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP613982.RA8aq4uOOC4TVr5mfca7FIjv5_jHsE8d6Eu0f6gLFrpNM
> .
@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:NP613982.RA8aq4uOOC4TVr5mfca7FIjv5_jHsE8d6Eu0f6gLFrpNM130_head
{
this:
np:hasAssertion
dgn-np:NP613982.RA8aq4uOOC4TVr5mfca7FIjv5_jHsE8d6Eu0f6gLFrpNM130_assertion
;
np:hasProvenance
dgn-np:NP613982.RA8aq4uOOC4TVr5mfca7FIjv5_jHsE8d6Eu0f6gLFrpNM130_provenance
;
np:hasPublicationInfo
dgn-np:NP613982.RA8aq4uOOC4TVr5mfca7FIjv5_jHsE8d6Eu0f6gLFrpNM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP613982.RA8aq4uOOC4TVr5mfca7FIjv5_jHsE8d6Eu0f6gLFrpNM130_assertion
a
np:Assertion
.
dgn-np:NP613982.RA8aq4uOOC4TVr5mfca7FIjv5_jHsE8d6Eu0f6gLFrpNM130_provenance
a
np:Provenance
.
dgn-np:NP613982.RA8aq4uOOC4TVr5mfca7FIjv5_jHsE8d6Eu0f6gLFrpNM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP613982.RA8aq4uOOC4TVr5mfca7FIjv5_jHsE8d6Eu0f6gLFrpNM130_assertion
{
miriam-gene:5444
a
ncit:C16612
.
lld:C0025286
a
ncit:C7057
.
dgn-gda:DGN7d77cbe023b4ee3491d79abb4a4cc613
sio:SIO_000628
miriam-gene:5444
,
lld:C0025286
;
a
sio:SIO_001121
.
}
dgn-np:NP613982.RA8aq4uOOC4TVr5mfca7FIjv5_jHsE8d6Eu0f6gLFrpNM130_provenance
{
dgn-np:NP613982.RA8aq4uOOC4TVr5mfca7FIjv5_jHsE8d6Eu0f6gLFrpNM130_assertion
dcterms:description
"[Aiming to identify genetic variations related to the risk of developing brain tumors, we investigated the putative association between common nonsynonymous PON1 polymorphisms and the risk of developing astrocytoma and meningioma.]. 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:20723250
;
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:NP613982.RA8aq4uOOC4TVr5mfca7FIjv5_jHsE8d6Eu0f6gLFrpNM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:11+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" .
}