@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP708577.RAE2O9Z8zjb0zthoEdhmLv8f0Bg6TaPdYcR7Xu9kRhtqg
> .
@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:NP708577.RAE2O9Z8zjb0zthoEdhmLv8f0Bg6TaPdYcR7Xu9kRhtqg130_head
{
this:
np:hasAssertion
dgn-np:NP708577.RAE2O9Z8zjb0zthoEdhmLv8f0Bg6TaPdYcR7Xu9kRhtqg130_assertion
;
np:hasProvenance
dgn-np:NP708577.RAE2O9Z8zjb0zthoEdhmLv8f0Bg6TaPdYcR7Xu9kRhtqg130_provenance
;
np:hasPublicationInfo
dgn-np:NP708577.RAE2O9Z8zjb0zthoEdhmLv8f0Bg6TaPdYcR7Xu9kRhtqg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP708577.RAE2O9Z8zjb0zthoEdhmLv8f0Bg6TaPdYcR7Xu9kRhtqg130_assertion
a
np:Assertion
.
dgn-np:NP708577.RAE2O9Z8zjb0zthoEdhmLv8f0Bg6TaPdYcR7Xu9kRhtqg130_provenance
a
np:Provenance
.
dgn-np:NP708577.RAE2O9Z8zjb0zthoEdhmLv8f0Bg6TaPdYcR7Xu9kRhtqg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP708577.RAE2O9Z8zjb0zthoEdhmLv8f0Bg6TaPdYcR7Xu9kRhtqg130_assertion
{
miriam-gene:5444
a
ncit:C16612
.
lld:C0042373
a
ncit:C7057
.
dgn-gda:DGN45fced5bd743b9a45b66ca72525a5dc9
sio:SIO_000628
miriam-gene:5444
,
lld:C0042373
;
a
sio:SIO_001121
.
}
dgn-np:NP708577.RAE2O9Z8zjb0zthoEdhmLv8f0Bg6TaPdYcR7Xu9kRhtqg130_provenance
{
dgn-np:NP708577.RAE2O9Z8zjb0zthoEdhmLv8f0Bg6TaPdYcR7Xu9kRhtqg130_assertion
dcterms:description
"[We determined both PON genotypes in 535 male individuals who were free of vascular disease and in 2249 male subjects who underwent coronary angiography, and analysed the relation of both gene variations to CAD and MI.]. 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:10998471
;
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:NP708577.RAE2O9Z8zjb0zthoEdhmLv8f0Bg6TaPdYcR7Xu9kRhtqg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:10+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" .
}