@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP968354.RA4uf-gWlq1CmW5jweBkJpaw2Meav_PPM0L_SFT51g9GI
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP968354.RA4uf-gWlq1CmW5jweBkJpaw2Meav_PPM0L_SFT51g9GI130_head
{
this:
np:hasAssertion
dgn-np:NP968354.RA4uf-gWlq1CmW5jweBkJpaw2Meav_PPM0L_SFT51g9GI130_assertion
;
np:hasProvenance
dgn-np:NP968354.RA4uf-gWlq1CmW5jweBkJpaw2Meav_PPM0L_SFT51g9GI130_provenance
;
np:hasPublicationInfo
dgn-np:NP968354.RA4uf-gWlq1CmW5jweBkJpaw2Meav_PPM0L_SFT51g9GI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP968354.RA4uf-gWlq1CmW5jweBkJpaw2Meav_PPM0L_SFT51g9GI130_assertion
a
np:Assertion
.
dgn-np:NP968354.RA4uf-gWlq1CmW5jweBkJpaw2Meav_PPM0L_SFT51g9GI130_provenance
a
np:Provenance
.
dgn-np:NP968354.RA4uf-gWlq1CmW5jweBkJpaw2Meav_PPM0L_SFT51g9GI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP968354.RA4uf-gWlq1CmW5jweBkJpaw2Meav_PPM0L_SFT51g9GI130_assertion
{
miriam-gene:124872
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGN05c1ec7956c8dfc1807061e3eae4e67b
sio:SIO_000628
miriam-gene:124872
,
lld:C0010054
;
a
sio:SIO_001121
.
}
dgn-np:NP968354.RA4uf-gWlq1CmW5jweBkJpaw2Meav_PPM0L_SFT51g9GI130_provenance
{
dgn-np:NP968354.RA4uf-gWlq1CmW5jweBkJpaw2Meav_PPM0L_SFT51g9GI130_assertion
dcterms:description
"[In the total sample and also in younger subjects, an association of the PON191 gene variation with the risk of CAD was not detected when the control group of individuals without coronary heart disease was compared with patients with at least one diseased vessel (verified by coronary angiography).]. 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-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP968354.RA4uf-gWlq1CmW5jweBkJpaw2Meav_PPM0L_SFT51g9GI130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:31+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}