@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP775399.RAcYn9oMvWVmcfOHGs-L7dyCbzRQ1uL1FLoAXI9bCirvo
> .
@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:NP775399.RAcYn9oMvWVmcfOHGs-L7dyCbzRQ1uL1FLoAXI9bCirvo130_head
{
this:
np:hasAssertion
dgn-np:NP775399.RAcYn9oMvWVmcfOHGs-L7dyCbzRQ1uL1FLoAXI9bCirvo130_assertion
;
np:hasProvenance
dgn-np:NP775399.RAcYn9oMvWVmcfOHGs-L7dyCbzRQ1uL1FLoAXI9bCirvo130_provenance
;
np:hasPublicationInfo
dgn-np:NP775399.RAcYn9oMvWVmcfOHGs-L7dyCbzRQ1uL1FLoAXI9bCirvo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP775399.RAcYn9oMvWVmcfOHGs-L7dyCbzRQ1uL1FLoAXI9bCirvo130_assertion
a
np:Assertion
.
dgn-np:NP775399.RAcYn9oMvWVmcfOHGs-L7dyCbzRQ1uL1FLoAXI9bCirvo130_provenance
a
np:Provenance
.
dgn-np:NP775399.RAcYn9oMvWVmcfOHGs-L7dyCbzRQ1uL1FLoAXI9bCirvo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP775399.RAcYn9oMvWVmcfOHGs-L7dyCbzRQ1uL1FLoAXI9bCirvo130_assertion
{
miriam-gene:255738
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGN07e217ca05189199501ecb74016ef163
sio:SIO_000628
miriam-gene:255738
,
lld:C0007222
;
a
sio:SIO_001121
.
}
dgn-np:NP775399.RAcYn9oMvWVmcfOHGs-L7dyCbzRQ1uL1FLoAXI9bCirvo130_provenance
{
dgn-np:NP775399.RAcYn9oMvWVmcfOHGs-L7dyCbzRQ1uL1FLoAXI9bCirvo130_assertion
dcterms:description
"[Our data support the concept that the rare allele of the R46L SNP at the PCSK9 locus significantly lowers LDL C, but does not greatly reduce CHD risk in an elderly population with a high prevalence of cardiovascular disease.]. 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:18262190
;
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:NP775399.RAcYn9oMvWVmcfOHGs-L7dyCbzRQ1uL1FLoAXI9bCirvo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:49+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" .
}