@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP570905.RA-ebTilXSRJ8vKjXFGiG9mn80Qfd5CAhUAsHygt62CpU
> .
@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:NP570905.RA-ebTilXSRJ8vKjXFGiG9mn80Qfd5CAhUAsHygt62CpU130_head
{
this:
np:hasAssertion
dgn-np:NP570905.RA-ebTilXSRJ8vKjXFGiG9mn80Qfd5CAhUAsHygt62CpU130_assertion
;
np:hasProvenance
dgn-np:NP570905.RA-ebTilXSRJ8vKjXFGiG9mn80Qfd5CAhUAsHygt62CpU130_provenance
;
np:hasPublicationInfo
dgn-np:NP570905.RA-ebTilXSRJ8vKjXFGiG9mn80Qfd5CAhUAsHygt62CpU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP570905.RA-ebTilXSRJ8vKjXFGiG9mn80Qfd5CAhUAsHygt62CpU130_assertion
a
np:Assertion
.
dgn-np:NP570905.RA-ebTilXSRJ8vKjXFGiG9mn80Qfd5CAhUAsHygt62CpU130_provenance
a
np:Provenance
.
dgn-np:NP570905.RA-ebTilXSRJ8vKjXFGiG9mn80Qfd5CAhUAsHygt62CpU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP570905.RA-ebTilXSRJ8vKjXFGiG9mn80Qfd5CAhUAsHygt62CpU130_assertion
{
miriam-gene:5444
a
ncit:C16612
.
lld:C0042373
a
ncit:C7057
.
dgn-gda:DGNfbf07c5225bb321c0d7e542bc073c16e
sio:SIO_000628
miriam-gene:5444
,
lld:C0042373
;
a
sio:SIO_001121
.
}
dgn-np:NP570905.RA-ebTilXSRJ8vKjXFGiG9mn80Qfd5CAhUAsHygt62CpU130_provenance
{
dgn-np:NP570905.RA-ebTilXSRJ8vKjXFGiG9mn80Qfd5CAhUAsHygt62CpU130_assertion
dcterms:description
"[The association of PON1 polymorphisms, lower PON1 activity and poorer diabetes control found in patients with macroangiopathy further support the idea of genetic factors contributing to the development of vascular disorders in diabetes.]. 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:17949258
;
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:NP570905.RA-ebTilXSRJ8vKjXFGiG9mn80Qfd5CAhUAsHygt62CpU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:44+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" .
}