@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP247979.RAwogYXYJwgtpDdhFRT4HtORtmFGHlySsEZisWJ3Gtoh8
> .
@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:NP247979.RAwogYXYJwgtpDdhFRT4HtORtmFGHlySsEZisWJ3Gtoh8130_head
{
this:
np:hasAssertion
dgn-np:NP247979.RAwogYXYJwgtpDdhFRT4HtORtmFGHlySsEZisWJ3Gtoh8130_assertion
;
np:hasProvenance
dgn-np:NP247979.RAwogYXYJwgtpDdhFRT4HtORtmFGHlySsEZisWJ3Gtoh8130_provenance
;
np:hasPublicationInfo
dgn-np:NP247979.RAwogYXYJwgtpDdhFRT4HtORtmFGHlySsEZisWJ3Gtoh8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP247979.RAwogYXYJwgtpDdhFRT4HtORtmFGHlySsEZisWJ3Gtoh8130_assertion
a
np:Assertion
.
dgn-np:NP247979.RAwogYXYJwgtpDdhFRT4HtORtmFGHlySsEZisWJ3Gtoh8130_provenance
a
np:Provenance
.
dgn-np:NP247979.RAwogYXYJwgtpDdhFRT4HtORtmFGHlySsEZisWJ3Gtoh8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP247979.RAwogYXYJwgtpDdhFRT4HtORtmFGHlySsEZisWJ3Gtoh8130_assertion
{
miriam-gene:4023
a
ncit:C16612
.
lld:C0151744
a
ncit:C7057
.
dgn-gda:DGNb1a6a00ecbb76fc9cc9879e215dfac33
sio:SIO_000628
miriam-gene:4023
,
lld:C0151744
;
a
sio:SIO_001121
.
}
dgn-np:NP247979.RAwogYXYJwgtpDdhFRT4HtORtmFGHlySsEZisWJ3Gtoh8130_provenance
{
dgn-np:NP247979.RAwogYXYJwgtpDdhFRT4HtORtmFGHlySsEZisWJ3Gtoh8130_assertion
dcterms:description
"[This study demonstrates that a single common mutation in the lipoprotein lipase gene is associated with elevated plasma triglycerides and reduced HDL cholesterol levels, whereby carriers, in particular women, seem to be predisposed to 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:9120004
;
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:NP247979.RAwogYXYJwgtpDdhFRT4HtORtmFGHlySsEZisWJ3Gtoh8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:18+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" .
}