@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP836721.RA9nsVi0vUIKe5Snz00HNkVWSC0DP2gm1Jh2-cb7OyjXI
> .
@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:NP836721.RA9nsVi0vUIKe5Snz00HNkVWSC0DP2gm1Jh2-cb7OyjXI130_head
{
this:
np:hasAssertion
dgn-np:NP836721.RA9nsVi0vUIKe5Snz00HNkVWSC0DP2gm1Jh2-cb7OyjXI130_assertion
;
np:hasProvenance
dgn-np:NP836721.RA9nsVi0vUIKe5Snz00HNkVWSC0DP2gm1Jh2-cb7OyjXI130_provenance
;
np:hasPublicationInfo
dgn-np:NP836721.RA9nsVi0vUIKe5Snz00HNkVWSC0DP2gm1Jh2-cb7OyjXI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP836721.RA9nsVi0vUIKe5Snz00HNkVWSC0DP2gm1Jh2-cb7OyjXI130_assertion
a
np:Assertion
.
dgn-np:NP836721.RA9nsVi0vUIKe5Snz00HNkVWSC0DP2gm1Jh2-cb7OyjXI130_provenance
a
np:Provenance
.
dgn-np:NP836721.RA9nsVi0vUIKe5Snz00HNkVWSC0DP2gm1Jh2-cb7OyjXI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP836721.RA9nsVi0vUIKe5Snz00HNkVWSC0DP2gm1Jh2-cb7OyjXI130_assertion
{
miriam-gene:10194
a
ncit:C16612
.
lld:C0497327
a
ncit:C7057
.
dgn-gda:DGNde1c3ca1cb263650f9ef2916ff45cac3
sio:SIO_000628
miriam-gene:10194
,
lld:C0497327
;
a
sio:SIO_001121
.
}
dgn-np:NP836721.RA9nsVi0vUIKe5Snz00HNkVWSC0DP2gm1Jh2-cb7OyjXI130_provenance
{
dgn-np:NP836721.RA9nsVi0vUIKe5Snz00HNkVWSC0DP2gm1Jh2-cb7OyjXI130_assertion
dcterms:description
"[CAA may contribute to the clinical presentation of dementia by interacting with other neuronal pathologies, leading to more severe cognitive impairment in men with both CAA and AD compared with men with only AD or CAA.]. 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:12058090
;
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:NP836721.RA9nsVi0vUIKe5Snz00HNkVWSC0DP2gm1Jh2-cb7OyjXI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:31+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" .
}