@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP133987.RApP5iuJgeCLM4NUfqshWcCfqDtLkgjmYrgqAkOS_S0bE
> .
@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:NP133987.RApP5iuJgeCLM4NUfqshWcCfqDtLkgjmYrgqAkOS_S0bE130_head
{
this:
np:hasAssertion
dgn-np:NP133987.RApP5iuJgeCLM4NUfqshWcCfqDtLkgjmYrgqAkOS_S0bE130_assertion
;
np:hasProvenance
dgn-np:NP133987.RApP5iuJgeCLM4NUfqshWcCfqDtLkgjmYrgqAkOS_S0bE130_provenance
;
np:hasPublicationInfo
dgn-np:NP133987.RApP5iuJgeCLM4NUfqshWcCfqDtLkgjmYrgqAkOS_S0bE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP133987.RApP5iuJgeCLM4NUfqshWcCfqDtLkgjmYrgqAkOS_S0bE130_assertion
a
np:Assertion
.
dgn-np:NP133987.RApP5iuJgeCLM4NUfqshWcCfqDtLkgjmYrgqAkOS_S0bE130_provenance
a
np:Provenance
.
dgn-np:NP133987.RApP5iuJgeCLM4NUfqshWcCfqDtLkgjmYrgqAkOS_S0bE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP133987.RApP5iuJgeCLM4NUfqshWcCfqDtLkgjmYrgqAkOS_S0bE130_assertion
{
miriam-gene:1071
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGN016dd2749eaf61de24f98814ee38bb59
sio:SIO_000628
miriam-gene:1071
,
lld:C1956346
;
a
sio:SIO_001122
.
}
dgn-np:NP133987.RApP5iuJgeCLM4NUfqshWcCfqDtLkgjmYrgqAkOS_S0bE130_provenance
{
dgn-np:NP133987.RApP5iuJgeCLM4NUfqshWcCfqDtLkgjmYrgqAkOS_S0bE130_assertion
dcterms:description
"[IVS14A and 451Q mutants of cholesteryl ester transfer protein (CETP) gene were rare in Chinese population and 442G mutant gene was possibly one of the susceptibility factors to Coronary Arteriosclerosis in Chinese.]. 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:12579494
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP133987.RApP5iuJgeCLM4NUfqshWcCfqDtLkgjmYrgqAkOS_S0bE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:09+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" .
}