@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP386573.RAbp_iCvd9iHIzm_3mzWhfmfaY8CQAjECs34DDTS-cKi4
> .
@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:NP386573.RAbp_iCvd9iHIzm_3mzWhfmfaY8CQAjECs34DDTS-cKi4130_head
{
this:
np:hasAssertion
dgn-np:NP386573.RAbp_iCvd9iHIzm_3mzWhfmfaY8CQAjECs34DDTS-cKi4130_assertion
;
np:hasProvenance
dgn-np:NP386573.RAbp_iCvd9iHIzm_3mzWhfmfaY8CQAjECs34DDTS-cKi4130_provenance
;
np:hasPublicationInfo
dgn-np:NP386573.RAbp_iCvd9iHIzm_3mzWhfmfaY8CQAjECs34DDTS-cKi4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP386573.RAbp_iCvd9iHIzm_3mzWhfmfaY8CQAjECs34DDTS-cKi4130_assertion
a
np:Assertion
.
dgn-np:NP386573.RAbp_iCvd9iHIzm_3mzWhfmfaY8CQAjECs34DDTS-cKi4130_provenance
a
np:Provenance
.
dgn-np:NP386573.RAbp_iCvd9iHIzm_3mzWhfmfaY8CQAjECs34DDTS-cKi4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP386573.RAbp_iCvd9iHIzm_3mzWhfmfaY8CQAjECs34DDTS-cKi4130_assertion
{
miriam-gene:336
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGNcd592fbc3bcd55b1a2023b4b91e89b8c
sio:SIO_000628
miriam-gene:336
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP386573.RAbp_iCvd9iHIzm_3mzWhfmfaY8CQAjECs34DDTS-cKi4130_provenance
{
dgn-np:NP386573.RAbp_iCvd9iHIzm_3mzWhfmfaY8CQAjECs34DDTS-cKi4130_assertion
dcterms:description
"[In a case-control analysis of 484 male CAD patients and 498 male controls, individuals carrying the 'CC' genotype for the APOAII rs5082 polymorphism had significantly lower risk of CAD than the 'T' allele carriers (OR=0.57, 95% CI 0.39-0.84, p=0.004).]. 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:18179799
;
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:NP386573.RAbp_iCvd9iHIzm_3mzWhfmfaY8CQAjECs34DDTS-cKi4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:50+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" .
}