@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP302568.RAkF7Pu8MRVhEyhK9GJFvu4pAmM9UkMcWqGhZN24O2Sxk
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP302568.RAkF7Pu8MRVhEyhK9GJFvu4pAmM9UkMcWqGhZN24O2Sxk130_head
{
this:
np:hasAssertion
dgn-np:NP302568.RAkF7Pu8MRVhEyhK9GJFvu4pAmM9UkMcWqGhZN24O2Sxk130_assertion
;
np:hasProvenance
dgn-np:NP302568.RAkF7Pu8MRVhEyhK9GJFvu4pAmM9UkMcWqGhZN24O2Sxk130_provenance
;
np:hasPublicationInfo
dgn-np:NP302568.RAkF7Pu8MRVhEyhK9GJFvu4pAmM9UkMcWqGhZN24O2Sxk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP302568.RAkF7Pu8MRVhEyhK9GJFvu4pAmM9UkMcWqGhZN24O2Sxk130_assertion
a
np:Assertion
.
dgn-np:NP302568.RAkF7Pu8MRVhEyhK9GJFvu4pAmM9UkMcWqGhZN24O2Sxk130_provenance
a
np:Provenance
.
dgn-np:NP302568.RAkF7Pu8MRVhEyhK9GJFvu4pAmM9UkMcWqGhZN24O2Sxk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP302568.RAkF7Pu8MRVhEyhK9GJFvu4pAmM9UkMcWqGhZN24O2Sxk130_assertion
{
miriam-gene:1071
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGN82c20260f0ec2cbbe088998ae4c6b5da
sio:SIO_000628
miriam-gene:1071
,
lld:C0010054
;
a
sio:SIO_001121
.
}
dgn-np:NP302568.RAkF7Pu8MRVhEyhK9GJFvu4pAmM9UkMcWqGhZN24O2Sxk130_provenance
{
dgn-np:NP302568.RAkF7Pu8MRVhEyhK9GJFvu4pAmM9UkMcWqGhZN24O2Sxk130_assertion
dcterms:description
"[Epidemiological studies in Japanese-Americans and in the Omagari area where HALP subjects with the intron 14 splicing defect of CETP gene are markedly frequent, have shown an increased incidence of coronary atherosclerosis in CETP-deficient patients.]. 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:11111094
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP302568.RAkF7Pu8MRVhEyhK9GJFvu4pAmM9UkMcWqGhZN24O2Sxk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:02+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}