@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP781302.RAHr0AtarEweAPwO4fFQ4hBTgL2zKBUA8uSBTG7bEpRZs
> .
@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:NP781302.RAHr0AtarEweAPwO4fFQ4hBTgL2zKBUA8uSBTG7bEpRZs130_head
{
this:
np:hasAssertion
dgn-np:NP781302.RAHr0AtarEweAPwO4fFQ4hBTgL2zKBUA8uSBTG7bEpRZs130_assertion
;
np:hasProvenance
dgn-np:NP781302.RAHr0AtarEweAPwO4fFQ4hBTgL2zKBUA8uSBTG7bEpRZs130_provenance
;
np:hasPublicationInfo
dgn-np:NP781302.RAHr0AtarEweAPwO4fFQ4hBTgL2zKBUA8uSBTG7bEpRZs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP781302.RAHr0AtarEweAPwO4fFQ4hBTgL2zKBUA8uSBTG7bEpRZs130_assertion
a
np:Assertion
.
dgn-np:NP781302.RAHr0AtarEweAPwO4fFQ4hBTgL2zKBUA8uSBTG7bEpRZs130_provenance
a
np:Provenance
.
dgn-np:NP781302.RAHr0AtarEweAPwO4fFQ4hBTgL2zKBUA8uSBTG7bEpRZs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP781302.RAHr0AtarEweAPwO4fFQ4hBTgL2zKBUA8uSBTG7bEpRZs130_assertion
{
miriam-gene:1071
a
ncit:C16612
.
lld:C0242339
a
ncit:C7057
.
dgn-gda:DGN9f5f1fd765a8afde393b00ee4456c457
sio:SIO_000628
miriam-gene:1071
,
lld:C0242339
;
a
sio:SIO_001121
.
}
dgn-np:NP781302.RAHr0AtarEweAPwO4fFQ4hBTgL2zKBUA8uSBTG7bEpRZs130_provenance
{
dgn-np:NP781302.RAHr0AtarEweAPwO4fFQ4hBTgL2zKBUA8uSBTG7bEpRZs130_assertion
dcterms:description
"[Single nucleotide polymorphisms (SNPs) and haplotypes in the CETP gene were determined in 98 patients with untreated dyslipidemias and analyzed for associations with plasma CETP and plasma lipids before and during statin treatment.]. 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:14583798
;
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:NP781302.RAHr0AtarEweAPwO4fFQ4hBTgL2zKBUA8uSBTG7bEpRZs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:53+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" .
}