@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP918467.RAvklnlfJi3i5gvcwDpD57x8b4oz-_R-VX8h42TxES6l4
> .
@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:NP918467.RAvklnlfJi3i5gvcwDpD57x8b4oz-_R-VX8h42TxES6l4130_head
{
this:
np:hasAssertion
dgn-np:NP918467.RAvklnlfJi3i5gvcwDpD57x8b4oz-_R-VX8h42TxES6l4130_assertion
;
np:hasProvenance
dgn-np:NP918467.RAvklnlfJi3i5gvcwDpD57x8b4oz-_R-VX8h42TxES6l4130_provenance
;
np:hasPublicationInfo
dgn-np:NP918467.RAvklnlfJi3i5gvcwDpD57x8b4oz-_R-VX8h42TxES6l4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP918467.RAvklnlfJi3i5gvcwDpD57x8b4oz-_R-VX8h42TxES6l4130_assertion
a
np:Assertion
.
dgn-np:NP918467.RAvklnlfJi3i5gvcwDpD57x8b4oz-_R-VX8h42TxES6l4130_provenance
a
np:Provenance
.
dgn-np:NP918467.RAvklnlfJi3i5gvcwDpD57x8b4oz-_R-VX8h42TxES6l4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP918467.RAvklnlfJi3i5gvcwDpD57x8b4oz-_R-VX8h42TxES6l4130_assertion
{
miriam-gene:146
a
ncit:C16612
.
lld:C0039292
a
ncit:C7057
.
dgn-gda:DGN371d55b9952933b7f4297084f966ecc8
sio:SIO_000628
miriam-gene:146
,
lld:C0039292
;
a
sio:SIO_001121
.
}
dgn-np:NP918467.RAvklnlfJi3i5gvcwDpD57x8b4oz-_R-VX8h42TxES6l4130_provenance
{
dgn-np:NP918467.RAvklnlfJi3i5gvcwDpD57x8b4oz-_R-VX8h42TxES6l4130_assertion
dcterms:description
"[We conclude that TD homozygotes have only prebeta(1) apoA-I-containing HDL subpopulations, while heterozygotes have HDL that is selectively depleted in the large alpha(1), prealpha(1), and alpha(2), prealpha(2) subpopulations, resulting in HDL particles that are small in size, poor in cholesterol, but relatively enriched in apoA-I compared to those of their unaffected relatives.]. 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:11369017
;
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:NP918467.RAvklnlfJi3i5gvcwDpD57x8b4oz-_R-VX8h42TxES6l4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:23+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" .
}