@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1282627.RAgCulLIrFxAsKd1x-n1Cmq9k9zpeytnAq6vu4XdqGVmE
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1282627.RAgCulLIrFxAsKd1x-n1Cmq9k9zpeytnAq6vu4XdqGVmE130_head
{
this:
np:hasAssertion
dgn-np:NP1282627.RAgCulLIrFxAsKd1x-n1Cmq9k9zpeytnAq6vu4XdqGVmE130_assertion
;
np:hasProvenance
dgn-np:NP1282627.RAgCulLIrFxAsKd1x-n1Cmq9k9zpeytnAq6vu4XdqGVmE130_provenance
;
np:hasPublicationInfo
dgn-np:NP1282627.RAgCulLIrFxAsKd1x-n1Cmq9k9zpeytnAq6vu4XdqGVmE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1282627.RAgCulLIrFxAsKd1x-n1Cmq9k9zpeytnAq6vu4XdqGVmE130_assertion
a
np:Assertion
.
dgn-np:NP1282627.RAgCulLIrFxAsKd1x-n1Cmq9k9zpeytnAq6vu4XdqGVmE130_provenance
a
np:Provenance
.
dgn-np:NP1282627.RAgCulLIrFxAsKd1x-n1Cmq9k9zpeytnAq6vu4XdqGVmE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1282627.RAgCulLIrFxAsKd1x-n1Cmq9k9zpeytnAq6vu4XdqGVmE130_assertion
{
miriam-gene:54209
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN482653e47c748201ba38555125c5d435
sio:SIO_000628
miriam-gene:54209
,
lld:C0002395
;
a
sio:SIO_001122
.
}
dgn-np:NP1282627.RAgCulLIrFxAsKd1x-n1Cmq9k9zpeytnAq6vu4XdqGVmE130_provenance
{
dgn-np:NP1282627.RAgCulLIrFxAsKd1x-n1Cmq9k9zpeytnAq6vu4XdqGVmE130_assertion
dcterms:description
"[Our findings, also supported by the β-amyloid plasma assay, confirm (1) the pathogenic role of the APP A713T mutation, (2) the specific phenotype (AD with cerebrovascular lesions) associated with this mutation, and (3) the large span of age at onset, not influenced by APOE, TOMM40, and TREM2 genes.]. 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:25948718
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1282627.RAgCulLIrFxAsKd1x-n1Cmq9k9zpeytnAq6vu4XdqGVmE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:27+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}