@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP48476.RAFDFDag1JOqPkkfgjh4hxvntj-wbJ-DWE_6C2sdmNbh4
> .
@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:NP48476.RAFDFDag1JOqPkkfgjh4hxvntj-wbJ-DWE_6C2sdmNbh4130_head
{
this:
np:hasAssertion
dgn-np:NP48476.RAFDFDag1JOqPkkfgjh4hxvntj-wbJ-DWE_6C2sdmNbh4130_assertion
;
np:hasProvenance
dgn-np:NP48476.RAFDFDag1JOqPkkfgjh4hxvntj-wbJ-DWE_6C2sdmNbh4130_provenance
;
np:hasPublicationInfo
dgn-np:NP48476.RAFDFDag1JOqPkkfgjh4hxvntj-wbJ-DWE_6C2sdmNbh4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP48476.RAFDFDag1JOqPkkfgjh4hxvntj-wbJ-DWE_6C2sdmNbh4130_assertion
a
np:Assertion
.
dgn-np:NP48476.RAFDFDag1JOqPkkfgjh4hxvntj-wbJ-DWE_6C2sdmNbh4130_provenance
a
np:Provenance
.
dgn-np:NP48476.RAFDFDag1JOqPkkfgjh4hxvntj-wbJ-DWE_6C2sdmNbh4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP48476.RAFDFDag1JOqPkkfgjh4hxvntj-wbJ-DWE_6C2sdmNbh4130_assertion
{
miriam-gene:335
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGN634e6a4fbe682606075cdac33ae3cbdd
sio:SIO_000628
miriam-gene:335
,
lld:C0010054
;
a
sio:SIO_001122
.
}
dgn-np:NP48476.RAFDFDag1JOqPkkfgjh4hxvntj-wbJ-DWE_6C2sdmNbh4130_provenance
{
dgn-np:NP48476.RAFDFDag1JOqPkkfgjh4hxvntj-wbJ-DWE_6C2sdmNbh4130_assertion
dcterms:description
"[ Our investigation reports the first evidence of an independent association of Lp(a) and apo(a) polymorphism with asymptomatic CAD. This suggests that Lp(a) levels and apo(a) phenotypes could be used together with other risk factors as markers of asymptomatic CAD in patients with 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:12145244
;
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:NP48476.RAFDFDag1JOqPkkfgjh4hxvntj-wbJ-DWE_6C2sdmNbh4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}