@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP564002.RAKMHQ6WPRa2eJHShDGx1xnR2uYiRNl2_Rl9sw05vDB50
> .
@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:NP564002.RAKMHQ6WPRa2eJHShDGx1xnR2uYiRNl2_Rl9sw05vDB50130_head
{
this:
np:hasAssertion
dgn-np:NP564002.RAKMHQ6WPRa2eJHShDGx1xnR2uYiRNl2_Rl9sw05vDB50130_assertion
;
np:hasProvenance
dgn-np:NP564002.RAKMHQ6WPRa2eJHShDGx1xnR2uYiRNl2_Rl9sw05vDB50130_provenance
;
np:hasPublicationInfo
dgn-np:NP564002.RAKMHQ6WPRa2eJHShDGx1xnR2uYiRNl2_Rl9sw05vDB50130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP564002.RAKMHQ6WPRa2eJHShDGx1xnR2uYiRNl2_Rl9sw05vDB50130_assertion
a
np:Assertion
.
dgn-np:NP564002.RAKMHQ6WPRa2eJHShDGx1xnR2uYiRNl2_Rl9sw05vDB50130_provenance
a
np:Provenance
.
dgn-np:NP564002.RAKMHQ6WPRa2eJHShDGx1xnR2uYiRNl2_Rl9sw05vDB50130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP564002.RAKMHQ6WPRa2eJHShDGx1xnR2uYiRNl2_Rl9sw05vDB50130_assertion
{
miriam-gene:213
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGNd93840ccb6384d4a186e2736a177c53b
sio:SIO_000628
miriam-gene:213
,
lld:C0007222
;
a
sio:SIO_001121
.
}
dgn-np:NP564002.RAKMHQ6WPRa2eJHShDGx1xnR2uYiRNl2_Rl9sw05vDB50130_provenance
{
dgn-np:NP564002.RAKMHQ6WPRa2eJHShDGx1xnR2uYiRNl2_Rl9sw05vDB50130_assertion
dcterms:description
"[In this study, we have investigated the possible effects of statins on the secretion of serum albumin from cultured HepG2 cells since high levels of serum albumin are associated with reduced risks for CVD and statins are effective in lowering the risk of CVD through other effects in addition to their effects on serum total cholesterol and LDL cholesterol levels, known as pleiotropic effects.]. 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:19291315
;
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:NP564002.RAKMHQ6WPRa2eJHShDGx1xnR2uYiRNl2_Rl9sw05vDB50130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:40+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" .
}