@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP892688.RAkodjB0FDhdVbJtyQBTKH487g4StBPDfKxxJYJb_ipuY
> .
@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:NP892688.RAkodjB0FDhdVbJtyQBTKH487g4StBPDfKxxJYJb_ipuY130_head
{
this:
np:hasAssertion
dgn-np:NP892688.RAkodjB0FDhdVbJtyQBTKH487g4StBPDfKxxJYJb_ipuY130_assertion
;
np:hasProvenance
dgn-np:NP892688.RAkodjB0FDhdVbJtyQBTKH487g4StBPDfKxxJYJb_ipuY130_provenance
;
np:hasPublicationInfo
dgn-np:NP892688.RAkodjB0FDhdVbJtyQBTKH487g4StBPDfKxxJYJb_ipuY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP892688.RAkodjB0FDhdVbJtyQBTKH487g4StBPDfKxxJYJb_ipuY130_assertion
a
np:Assertion
.
dgn-np:NP892688.RAkodjB0FDhdVbJtyQBTKH487g4StBPDfKxxJYJb_ipuY130_provenance
a
np:Provenance
.
dgn-np:NP892688.RAkodjB0FDhdVbJtyQBTKH487g4StBPDfKxxJYJb_ipuY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP892688.RAkodjB0FDhdVbJtyQBTKH487g4StBPDfKxxJYJb_ipuY130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0342880
a
ncit:C7057
.
dgn-gda:DGN434bd0848f7ec535bbe5ffc26e3168cc
sio:SIO_000628
miriam-gene:348
,
lld:C0342880
;
a
sio:SIO_001121
.
}
dgn-np:NP892688.RAkodjB0FDhdVbJtyQBTKH487g4StBPDfKxxJYJb_ipuY130_provenance
{
dgn-np:NP892688.RAkodjB0FDhdVbJtyQBTKH487g4StBPDfKxxJYJb_ipuY130_assertion
dcterms:description
"[This may explain the observed significant effects of the apoE alleles on the phenotypic variance of plasma lipoprotein concentrations in different ethnic groups and, moreover, the involvement of apoE alleles in the pathogenesis of multifactorial forms of hyperlipidaemia, for example, hypertriglyceridaemia, familial type III hyperlipidaemia (apoE-2 Arg-158----Cys) and polygenic hypercholesterolaemia (apoE-4 Cys-112----Arg).]. 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:2965000
;
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:NP892688.RAkodjB0FDhdVbJtyQBTKH487g4StBPDfKxxJYJb_ipuY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:08+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" .
}