@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP717639.RA64FnFZr8JpOXbG05cVZTZpqLL3gTfZXvc6DCt_E_sjs
> .
@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:NP717639.RA64FnFZr8JpOXbG05cVZTZpqLL3gTfZXvc6DCt_E_sjs130_head
{
this:
np:hasAssertion
dgn-np:NP717639.RA64FnFZr8JpOXbG05cVZTZpqLL3gTfZXvc6DCt_E_sjs130_assertion
;
np:hasProvenance
dgn-np:NP717639.RA64FnFZr8JpOXbG05cVZTZpqLL3gTfZXvc6DCt_E_sjs130_provenance
;
np:hasPublicationInfo
dgn-np:NP717639.RA64FnFZr8JpOXbG05cVZTZpqLL3gTfZXvc6DCt_E_sjs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP717639.RA64FnFZr8JpOXbG05cVZTZpqLL3gTfZXvc6DCt_E_sjs130_assertion
a
np:Assertion
.
dgn-np:NP717639.RA64FnFZr8JpOXbG05cVZTZpqLL3gTfZXvc6DCt_E_sjs130_provenance
a
np:Provenance
.
dgn-np:NP717639.RA64FnFZr8JpOXbG05cVZTZpqLL3gTfZXvc6DCt_E_sjs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP717639.RA64FnFZr8JpOXbG05cVZTZpqLL3gTfZXvc6DCt_E_sjs130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0342883
a
ncit:C7057
.
dgn-gda:DGN175f9d644dd6fe08c7997020dbd7a65e
sio:SIO_000628
miriam-gene:348
,
lld:C0342883
;
a
sio:SIO_001121
.
}
dgn-np:NP717639.RA64FnFZr8JpOXbG05cVZTZpqLL3gTfZXvc6DCt_E_sjs130_provenance
{
dgn-np:NP717639.RA64FnFZr8JpOXbG05cVZTZpqLL3gTfZXvc6DCt_E_sjs130_assertion
dcterms:description
"[We conclude that hyperalphalipoproteinemia due to complete deficiency of cholesteryl ester transfer activity is characterized by the presence of both small polydisperse LDL and markedly large HDL enriched with cholesteryl ester and apolipoprotein E.]. 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:3355618
;
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:NP717639.RA64FnFZr8JpOXbG05cVZTZpqLL3gTfZXvc6DCt_E_sjs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:16+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" .
}