@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP62166.RA2HEiKRrcR-a7UrKwAC0w6xD2bYXibu8w1plX-MNP_Hg
> .
@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:NP62166.RA2HEiKRrcR-a7UrKwAC0w6xD2bYXibu8w1plX-MNP_Hg130_head
{
this:
np:hasAssertion
dgn-np:NP62166.RA2HEiKRrcR-a7UrKwAC0w6xD2bYXibu8w1plX-MNP_Hg130_assertion
;
np:hasProvenance
dgn-np:NP62166.RA2HEiKRrcR-a7UrKwAC0w6xD2bYXibu8w1plX-MNP_Hg130_provenance
;
np:hasPublicationInfo
dgn-np:NP62166.RA2HEiKRrcR-a7UrKwAC0w6xD2bYXibu8w1plX-MNP_Hg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP62166.RA2HEiKRrcR-a7UrKwAC0w6xD2bYXibu8w1plX-MNP_Hg130_assertion
a
np:Assertion
.
dgn-np:NP62166.RA2HEiKRrcR-a7UrKwAC0w6xD2bYXibu8w1plX-MNP_Hg130_provenance
a
np:Provenance
.
dgn-np:NP62166.RA2HEiKRrcR-a7UrKwAC0w6xD2bYXibu8w1plX-MNP_Hg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP62166.RA2HEiKRrcR-a7UrKwAC0w6xD2bYXibu8w1plX-MNP_Hg130_assertion
{
miriam-gene:23385
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGNbeb60b1ae63929c9fa76763c259cb3b5
sio:SIO_000628
miriam-gene:23385
,
lld:C0002395
;
a
sio:SIO_001122
.
}
dgn-np:NP62166.RA2HEiKRrcR-a7UrKwAC0w6xD2bYXibu8w1plX-MNP_Hg130_provenance
{
dgn-np:NP62166.RA2HEiKRrcR-a7UrKwAC0w6xD2bYXibu8w1plX-MNP_Hg130_assertion
dcterms:description
"[No evidence of association was obtained between the two SNPs investigated in sporadic and familial AD cases under the stratification of currently known genetic risk factors including the apolipoprotein E (APOE), the presenilins and the beta-amyloid precursor protein. The result suggests no apparent synergic interaction between the NCSTN and APOE varepsilon 4 in the risk to develop the late onset sporadic form of AD. But considering its biological effects, the result can not exclude the NCSTN as candidate for genetic factor in AD. Further genetic study of the NCSTN would be necessary to evaluate the potential genetic involvement in 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:12419494
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP62166.RA2HEiKRrcR-a7UrKwAC0w6xD2bYXibu8w1plX-MNP_Hg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:29+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" .
}