@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP756597.RAuakkvaWTXFyfa2nIDQ7iXDL2NApuAcrm7TG0eKTrvHo
> .
@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:NP756597.RAuakkvaWTXFyfa2nIDQ7iXDL2NApuAcrm7TG0eKTrvHo130_head
{
this:
np:hasAssertion
dgn-np:NP756597.RAuakkvaWTXFyfa2nIDQ7iXDL2NApuAcrm7TG0eKTrvHo130_assertion
;
np:hasProvenance
dgn-np:NP756597.RAuakkvaWTXFyfa2nIDQ7iXDL2NApuAcrm7TG0eKTrvHo130_provenance
;
np:hasPublicationInfo
dgn-np:NP756597.RAuakkvaWTXFyfa2nIDQ7iXDL2NApuAcrm7TG0eKTrvHo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP756597.RAuakkvaWTXFyfa2nIDQ7iXDL2NApuAcrm7TG0eKTrvHo130_assertion
a
np:Assertion
.
dgn-np:NP756597.RAuakkvaWTXFyfa2nIDQ7iXDL2NApuAcrm7TG0eKTrvHo130_provenance
a
np:Provenance
.
dgn-np:NP756597.RAuakkvaWTXFyfa2nIDQ7iXDL2NApuAcrm7TG0eKTrvHo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP756597.RAuakkvaWTXFyfa2nIDQ7iXDL2NApuAcrm7TG0eKTrvHo130_assertion
{
miriam-gene:3990
a
ncit:C16612
.
lld:C0342883
a
ncit:C7057
.
dgn-gda:DGNae9ae612ed9ccaa2547bc9337fb27f17
sio:SIO_000628
miriam-gene:3990
,
lld:C0342883
;
a
sio:SIO_001121
.
}
dgn-np:NP756597.RAuakkvaWTXFyfa2nIDQ7iXDL2NApuAcrm7TG0eKTrvHo130_provenance
{
dgn-np:NP756597.RAuakkvaWTXFyfa2nIDQ7iXDL2NApuAcrm7TG0eKTrvHo130_assertion
dcterms:description
"[To further clarify the characteristics of marked HALP in patients with ACD, we compared the plasma lipids, lipoproteins, CETP, and HTGL activities between heterozygotes for CETP deficiency who were with and without ACD.]. 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:7583564
;
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:NP756597.RAuakkvaWTXFyfa2nIDQ7iXDL2NApuAcrm7TG0eKTrvHo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:38+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" .
}