@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP637958.RAcM6R5ee-y2DbRFcPQGAuZHQCvd2hzxmchizH_ylDUr0
> .
@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:NP637958.RAcM6R5ee-y2DbRFcPQGAuZHQCvd2hzxmchizH_ylDUr0130_head
{
this:
np:hasAssertion
dgn-np:NP637958.RAcM6R5ee-y2DbRFcPQGAuZHQCvd2hzxmchizH_ylDUr0130_assertion
;
np:hasProvenance
dgn-np:NP637958.RAcM6R5ee-y2DbRFcPQGAuZHQCvd2hzxmchizH_ylDUr0130_provenance
;
np:hasPublicationInfo
dgn-np:NP637958.RAcM6R5ee-y2DbRFcPQGAuZHQCvd2hzxmchizH_ylDUr0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP637958.RAcM6R5ee-y2DbRFcPQGAuZHQCvd2hzxmchizH_ylDUr0130_assertion
a
np:Assertion
.
dgn-np:NP637958.RAcM6R5ee-y2DbRFcPQGAuZHQCvd2hzxmchizH_ylDUr0130_provenance
a
np:Provenance
.
dgn-np:NP637958.RAcM6R5ee-y2DbRFcPQGAuZHQCvd2hzxmchizH_ylDUr0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP637958.RAcM6R5ee-y2DbRFcPQGAuZHQCvd2hzxmchizH_ylDUr0130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C3494652
a
ncit:C7057
.
dgn-gda:DGNcf21336f2653e49d5ba374b176228717
sio:SIO_000628
miriam-gene:348
,
lld:C3494652
;
a
sio:SIO_001121
.
}
dgn-np:NP637958.RAcM6R5ee-y2DbRFcPQGAuZHQCvd2hzxmchizH_ylDUr0130_provenance
{
dgn-np:NP637958.RAcM6R5ee-y2DbRFcPQGAuZHQCvd2hzxmchizH_ylDUr0130_assertion
dcterms:description
"[The ApoCI A allele was associated with AD of moderate to severe dementia when patients were divided into two subgroups according to Clinical Dementia Rating scale, and the AA genotype was strongly associated with moderate to severe AD in ApoE epsilon4 allele carriers [odds ratio (OR) = 8.19, 95% confidential interval: 1.28-52.30, after adjusting for age and gender by logistic regression analysis], although in total no significant differences of allele or genotype frequency between patients and controls were found.]. 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:14705977
;
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:NP637958.RAcM6R5ee-y2DbRFcPQGAuZHQCvd2hzxmchizH_ylDUr0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:25+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" .
}