@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP46924.RA2OlzqmtOOauMwUj82UVJtzMNg8a3kWWvxlE9nPNFgGI
> .
@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:NP46924.RA2OlzqmtOOauMwUj82UVJtzMNg8a3kWWvxlE9nPNFgGI130_head
{
this:
np:hasAssertion
dgn-np:NP46924.RA2OlzqmtOOauMwUj82UVJtzMNg8a3kWWvxlE9nPNFgGI130_assertion
;
np:hasProvenance
dgn-np:NP46924.RA2OlzqmtOOauMwUj82UVJtzMNg8a3kWWvxlE9nPNFgGI130_provenance
;
np:hasPublicationInfo
dgn-np:NP46924.RA2OlzqmtOOauMwUj82UVJtzMNg8a3kWWvxlE9nPNFgGI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP46924.RA2OlzqmtOOauMwUj82UVJtzMNg8a3kWWvxlE9nPNFgGI130_assertion
a
np:Assertion
.
dgn-np:NP46924.RA2OlzqmtOOauMwUj82UVJtzMNg8a3kWWvxlE9nPNFgGI130_provenance
a
np:Provenance
.
dgn-np:NP46924.RA2OlzqmtOOauMwUj82UVJtzMNg8a3kWWvxlE9nPNFgGI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP46924.RA2OlzqmtOOauMwUj82UVJtzMNg8a3kWWvxlE9nPNFgGI130_assertion
{
miriam-gene:1071
a
ncit:C16612
.
lld:C0027051
a
ncit:C7057
.
dgn-gda:DGN7ef94c2ad35ce827bff320fd325e3950
sio:SIO_000628
miriam-gene:1071
,
lld:C0027051
;
a
sio:SIO_001122
.
}
dgn-np:NP46924.RA2OlzqmtOOauMwUj82UVJtzMNg8a3kWWvxlE9nPNFgGI130_provenance
{
dgn-np:NP46924.RA2OlzqmtOOauMwUj82UVJtzMNg8a3kWWvxlE9nPNFgGI130_assertion
dcterms:description
"[These results strongly confirm the role of the CETP gene and the TaqIB variant as a risk factor for MI and suggest that another functional polymorphism is yet to be discovered in the CETP gene, that will explain the effect on MI associated with TaqIB observed in this study.]. 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:11689220
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP46924.RA2OlzqmtOOauMwUj82UVJtzMNg8a3kWWvxlE9nPNFgGI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:21+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" .
}