@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP320006.RAKfo-RVU21Jpt7LDMUQbZ43O2N12cqkwwGI9FPmhu1p8
> .
@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:NP320006.RAKfo-RVU21Jpt7LDMUQbZ43O2N12cqkwwGI9FPmhu1p8130_head
{
this:
np:hasAssertion
dgn-np:NP320006.RAKfo-RVU21Jpt7LDMUQbZ43O2N12cqkwwGI9FPmhu1p8130_assertion
;
np:hasProvenance
dgn-np:NP320006.RAKfo-RVU21Jpt7LDMUQbZ43O2N12cqkwwGI9FPmhu1p8130_provenance
;
np:hasPublicationInfo
dgn-np:NP320006.RAKfo-RVU21Jpt7LDMUQbZ43O2N12cqkwwGI9FPmhu1p8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP320006.RAKfo-RVU21Jpt7LDMUQbZ43O2N12cqkwwGI9FPmhu1p8130_assertion
a
np:Assertion
.
dgn-np:NP320006.RAKfo-RVU21Jpt7LDMUQbZ43O2N12cqkwwGI9FPmhu1p8130_provenance
a
np:Provenance
.
dgn-np:NP320006.RAKfo-RVU21Jpt7LDMUQbZ43O2N12cqkwwGI9FPmhu1p8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP320006.RAKfo-RVU21Jpt7LDMUQbZ43O2N12cqkwwGI9FPmhu1p8130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0948089
a
ncit:C7057
.
dgn-gda:DGNf1b0757b0894eadd3bbfbf061484dae9
sio:SIO_000628
miriam-gene:348
,
lld:C0948089
;
a
sio:SIO_001121
.
}
dgn-np:NP320006.RAKfo-RVU21Jpt7LDMUQbZ43O2N12cqkwwGI9FPmhu1p8130_provenance
{
dgn-np:NP320006.RAKfo-RVU21Jpt7LDMUQbZ43O2N12cqkwwGI9FPmhu1p8130_assertion
dcterms:description
"[This was a cross-sectional, multicenter study with 207 patients (138 men), with acute coronary syndrome (ACS), in the city of Niteroi, state of Rio de Janeiro, Brazil, who underwent coronary angiography and genotype determination for the APOE *2*3*4 polymorphism by the Restriction Fragment Length Polymorphism (RFLP) method.]. 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:19851649
;
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:NP320006.RAKfo-RVU21Jpt7LDMUQbZ43O2N12cqkwwGI9FPmhu1p8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:05+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" .
}