@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP781739.RAYsxWdtkU4X6WjDr2NIODwE47lpH_b-vyTy1qFelIJSA
> .
@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:NP781739.RAYsxWdtkU4X6WjDr2NIODwE47lpH_b-vyTy1qFelIJSA130_head
{
this:
np:hasAssertion
dgn-np:NP781739.RAYsxWdtkU4X6WjDr2NIODwE47lpH_b-vyTy1qFelIJSA130_assertion
;
np:hasProvenance
dgn-np:NP781739.RAYsxWdtkU4X6WjDr2NIODwE47lpH_b-vyTy1qFelIJSA130_provenance
;
np:hasPublicationInfo
dgn-np:NP781739.RAYsxWdtkU4X6WjDr2NIODwE47lpH_b-vyTy1qFelIJSA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP781739.RAYsxWdtkU4X6WjDr2NIODwE47lpH_b-vyTy1qFelIJSA130_assertion
a
np:Assertion
.
dgn-np:NP781739.RAYsxWdtkU4X6WjDr2NIODwE47lpH_b-vyTy1qFelIJSA130_provenance
a
np:Provenance
.
dgn-np:NP781739.RAYsxWdtkU4X6WjDr2NIODwE47lpH_b-vyTy1qFelIJSA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP781739.RAYsxWdtkU4X6WjDr2NIODwE47lpH_b-vyTy1qFelIJSA130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0162871
a
ncit:C7057
.
dgn-gda:DGN2dafa2b824ed830d2696024ebfa5fc0f
sio:SIO_000628
miriam-gene:348
,
lld:C0162871
;
a
sio:SIO_001121
.
}
dgn-np:NP781739.RAYsxWdtkU4X6WjDr2NIODwE47lpH_b-vyTy1qFelIJSA130_provenance
{
dgn-np:NP781739.RAYsxWdtkU4X6WjDr2NIODwE47lpH_b-vyTy1qFelIJSA130_assertion
dcterms:description
"[APOE genotype seems to influence AAA expansion rate, but the effects of the individual genotypes, in particular E3E3 and E3E4, are contradictory when compared with the effects of the genotypes on risk of atherosclerosis.]. 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:10848855
;
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:NP781739.RAYsxWdtkU4X6WjDr2NIODwE47lpH_b-vyTy1qFelIJSA130_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" .
}