@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP761328.RAOrPSASWxpesIshZ3SEcGHqENRkLbaRWN038ATE1QQLE
> .
@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:NP761328.RAOrPSASWxpesIshZ3SEcGHqENRkLbaRWN038ATE1QQLE130_head
{
this:
np:hasAssertion
dgn-np:NP761328.RAOrPSASWxpesIshZ3SEcGHqENRkLbaRWN038ATE1QQLE130_assertion
;
np:hasProvenance
dgn-np:NP761328.RAOrPSASWxpesIshZ3SEcGHqENRkLbaRWN038ATE1QQLE130_provenance
;
np:hasPublicationInfo
dgn-np:NP761328.RAOrPSASWxpesIshZ3SEcGHqENRkLbaRWN038ATE1QQLE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP761328.RAOrPSASWxpesIshZ3SEcGHqENRkLbaRWN038ATE1QQLE130_assertion
a
np:Assertion
.
dgn-np:NP761328.RAOrPSASWxpesIshZ3SEcGHqENRkLbaRWN038ATE1QQLE130_provenance
a
np:Provenance
.
dgn-np:NP761328.RAOrPSASWxpesIshZ3SEcGHqENRkLbaRWN038ATE1QQLE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP761328.RAOrPSASWxpesIshZ3SEcGHqENRkLbaRWN038ATE1QQLE130_assertion
{
miriam-gene:788
a
ncit:C16612
.
lld:C0007785
a
ncit:C7057
.
dgn-gda:DGN743763690829d8dbf2dd5dc2b9294aa8
sio:SIO_000628
miriam-gene:788
,
lld:C0007785
;
a
sio:SIO_001121
.
}
dgn-np:NP761328.RAOrPSASWxpesIshZ3SEcGHqENRkLbaRWN038ATE1QQLE130_provenance
{
dgn-np:NP761328.RAOrPSASWxpesIshZ3SEcGHqENRkLbaRWN038ATE1QQLE130_assertion
dcterms:description
"[Subjects with higher CAC were more likely to have dementia and lower cognitive scores, more likely to have lower white matter volume, gray matter volume, and total brain tissue, and to have more cerebral infarcts, cerebral microbleeds, and white matter lesions.]. 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:20360538
;
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:NP761328.RAOrPSASWxpesIshZ3SEcGHqENRkLbaRWN038ATE1QQLE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:41+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" .
}