@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1381474.RAu7JQ2wxmKTJ1pmuWWlPw_JovYd4kwNfo6Lz67MaCJYI
> .
@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/v4.0.0/void/
> .
dgn-np:NP1381474.RAu7JQ2wxmKTJ1pmuWWlPw_JovYd4kwNfo6Lz67MaCJYI130_head
{
this:
np:hasAssertion
dgn-np:NP1381474.RAu7JQ2wxmKTJ1pmuWWlPw_JovYd4kwNfo6Lz67MaCJYI130_assertion
;
np:hasProvenance
dgn-np:NP1381474.RAu7JQ2wxmKTJ1pmuWWlPw_JovYd4kwNfo6Lz67MaCJYI130_provenance
;
np:hasPublicationInfo
dgn-np:NP1381474.RAu7JQ2wxmKTJ1pmuWWlPw_JovYd4kwNfo6Lz67MaCJYI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1381474.RAu7JQ2wxmKTJ1pmuWWlPw_JovYd4kwNfo6Lz67MaCJYI130_assertion
a
np:Assertion
.
dgn-np:NP1381474.RAu7JQ2wxmKTJ1pmuWWlPw_JovYd4kwNfo6Lz67MaCJYI130_provenance
a
np:Provenance
.
dgn-np:NP1381474.RAu7JQ2wxmKTJ1pmuWWlPw_JovYd4kwNfo6Lz67MaCJYI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1381474.RAu7JQ2wxmKTJ1pmuWWlPw_JovYd4kwNfo6Lz67MaCJYI130_assertion
{
miriam-gene:4023
a
ncit:C16612
.
lld:C0030305
a
ncit:C7057
.
dgn-gda:DGN5eea865bd0baa927353c5a8bd0acd5da
sio:SIO_000628
miriam-gene:4023
,
lld:C0030305
;
a
sio:SIO_001121
.
}
dgn-np:NP1381474.RAu7JQ2wxmKTJ1pmuWWlPw_JovYd4kwNfo6Lz67MaCJYI130_provenance
{
dgn-np:NP1381474.RAu7JQ2wxmKTJ1pmuWWlPw_JovYd4kwNfo6Lz67MaCJYI130_assertion
dcterms:description
"[Patients with mutations on both alleles of the lipoprotein lipase gene resulting in complete lipoprotein lipase deficiency exhibit the chylomicronemia syndrome with severe hypertriglyceridemia and increased risk of pancreatitis and possibly of ischemic heart 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:9323055
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1381474.RAu7JQ2wxmKTJ1pmuWWlPw_JovYd4kwNfo6Lz67MaCJYI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:12+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}