@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg
> .
@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:NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_head
{
this:
np:hasAssertion
dgn-np:NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_assertion
;
np:hasProvenance
dgn-np:NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_provenance
;
np:hasPublicationInfo
dgn-np:NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_assertion
a
np:Assertion
.
dgn-np:NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_provenance
a
np:Provenance
.
dgn-np:NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0025362
a
ncit:C7057
.
dgn-gda:DGN0bc6dac537712000923a45bdeeb95848
sio:SIO_000628
miriam-gene:348
,
lld:C0025362
;
a
sio:SIO_001121
.
}
dgn-np:NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_provenance
{
dgn-np:NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_assertion
dcterms:description
"[We studied the allelic frequencies of ApoE in 26 DS cases fulfilling clinical diagnostic criteria for AD and in 26 DS controls matched for age, sex, and premorbid level of mental retardation.]. 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:7654070
;
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:NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:29+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" .
}