@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP324254.RAQLVWgIEQcwOlg1twW-sXH6sJ7fSSGQHEdi9Lk2VhSic
> .
@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:NP324254.RAQLVWgIEQcwOlg1twW-sXH6sJ7fSSGQHEdi9Lk2VhSic130_head
{
this:
np:hasAssertion
dgn-np:NP324254.RAQLVWgIEQcwOlg1twW-sXH6sJ7fSSGQHEdi9Lk2VhSic130_assertion
;
np:hasProvenance
dgn-np:NP324254.RAQLVWgIEQcwOlg1twW-sXH6sJ7fSSGQHEdi9Lk2VhSic130_provenance
;
np:hasPublicationInfo
dgn-np:NP324254.RAQLVWgIEQcwOlg1twW-sXH6sJ7fSSGQHEdi9Lk2VhSic130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP324254.RAQLVWgIEQcwOlg1twW-sXH6sJ7fSSGQHEdi9Lk2VhSic130_assertion
a
np:Assertion
.
dgn-np:NP324254.RAQLVWgIEQcwOlg1twW-sXH6sJ7fSSGQHEdi9Lk2VhSic130_provenance
a
np:Provenance
.
dgn-np:NP324254.RAQLVWgIEQcwOlg1twW-sXH6sJ7fSSGQHEdi9Lk2VhSic130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP324254.RAQLVWgIEQcwOlg1twW-sXH6sJ7fSSGQHEdi9Lk2VhSic130_assertion
{
miriam-gene:1636
a
ncit:C16612
.
lld:C0011854
a
ncit:C7057
.
dgn-gda:DGN78fa0e477cffc0354ab04d5abb4683ed
sio:SIO_000628
miriam-gene:1636
,
lld:C0011854
;
a
sio:SIO_001121
.
}
dgn-np:NP324254.RAQLVWgIEQcwOlg1twW-sXH6sJ7fSSGQHEdi9Lk2VhSic130_provenance
{
dgn-np:NP324254.RAQLVWgIEQcwOlg1twW-sXH6sJ7fSSGQHEdi9Lk2VhSic130_assertion
dcterms:description
"[Specific polymorphisms of the apolipoprotein E (APOE) and angiotensin-converting enzyme (ACE) genes appear to increase risk for Alzheimer's disease and cognitive dysfunction in the general population, yet little research has examined whether genetic factors influence risk of cognitive dysfunction in patients with Type 1 diabetes.]. 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:20121884
;
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:NP324254.RAQLVWgIEQcwOlg1twW-sXH6sJ7fSSGQHEdi9Lk2VhSic130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:09+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" .
}