@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP148922.RAYLm7IGjW9_xx7rrASCvtvIMaNM1J5dBmhJA0mE9oFvs
> .
@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:NP148922.RAYLm7IGjW9_xx7rrASCvtvIMaNM1J5dBmhJA0mE9oFvs130_head
{
this:
np:hasAssertion
dgn-np:NP148922.RAYLm7IGjW9_xx7rrASCvtvIMaNM1J5dBmhJA0mE9oFvs130_assertion
;
np:hasProvenance
dgn-np:NP148922.RAYLm7IGjW9_xx7rrASCvtvIMaNM1J5dBmhJA0mE9oFvs130_provenance
;
np:hasPublicationInfo
dgn-np:NP148922.RAYLm7IGjW9_xx7rrASCvtvIMaNM1J5dBmhJA0mE9oFvs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP148922.RAYLm7IGjW9_xx7rrASCvtvIMaNM1J5dBmhJA0mE9oFvs130_assertion
a
np:Assertion
.
dgn-np:NP148922.RAYLm7IGjW9_xx7rrASCvtvIMaNM1J5dBmhJA0mE9oFvs130_provenance
a
np:Provenance
.
dgn-np:NP148922.RAYLm7IGjW9_xx7rrASCvtvIMaNM1J5dBmhJA0mE9oFvs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP148922.RAYLm7IGjW9_xx7rrASCvtvIMaNM1J5dBmhJA0mE9oFvs130_assertion
{
miriam-gene:5445
a
ncit:C16612
.
lld:C0497327
a
ncit:C7057
.
dgn-gda:DGNf04159d2d1b6b916a8a28e43386ab5d0
sio:SIO_000628
miriam-gene:5445
,
lld:C0497327
;
a
sio:SIO_001122
.
}
dgn-np:NP148922.RAYLm7IGjW9_xx7rrASCvtvIMaNM1J5dBmhJA0mE9oFvs130_provenance
{
dgn-np:NP148922.RAYLm7IGjW9_xx7rrASCvtvIMaNM1J5dBmhJA0mE9oFvs130_assertion
dcterms:description
"[PON2*S and apoE4 alleles have interactive effect on the development of the two most common forms of dementias AD and VD, and further support the hypothesis that cardiovascular factors contribute to the development of AD.]. 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:11803456
;
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:NP148922.RAYLm7IGjW9_xx7rrASCvtvIMaNM1J5dBmhJA0mE9oFvs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:19+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" .
}