@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP460188.RASrQATiojZezdUTvspLnj9dFJWs5guJ6oTWQ0rnk8TM0
> .
@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:NP460188.RASrQATiojZezdUTvspLnj9dFJWs5guJ6oTWQ0rnk8TM0130_head
{
this:
np:hasAssertion
dgn-np:NP460188.RASrQATiojZezdUTvspLnj9dFJWs5guJ6oTWQ0rnk8TM0130_assertion
;
np:hasProvenance
dgn-np:NP460188.RASrQATiojZezdUTvspLnj9dFJWs5guJ6oTWQ0rnk8TM0130_provenance
;
np:hasPublicationInfo
dgn-np:NP460188.RASrQATiojZezdUTvspLnj9dFJWs5guJ6oTWQ0rnk8TM0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP460188.RASrQATiojZezdUTvspLnj9dFJWs5guJ6oTWQ0rnk8TM0130_assertion
a
np:Assertion
.
dgn-np:NP460188.RASrQATiojZezdUTvspLnj9dFJWs5guJ6oTWQ0rnk8TM0130_provenance
a
np:Provenance
.
dgn-np:NP460188.RASrQATiojZezdUTvspLnj9dFJWs5guJ6oTWQ0rnk8TM0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP460188.RASrQATiojZezdUTvspLnj9dFJWs5guJ6oTWQ0rnk8TM0130_assertion
{
miriam-gene:351
a
ncit:C16612
.
lld:C0238190
a
ncit:C7057
.
dgn-gda:DGNad67043d60e7c46cb392471a0456cbba
sio:SIO_000628
miriam-gene:351
,
lld:C0238190
;
a
sio:SIO_001121
.
}
dgn-np:NP460188.RASrQATiojZezdUTvspLnj9dFJWs5guJ6oTWQ0rnk8TM0130_provenance
{
dgn-np:NP460188.RASrQATiojZezdUTvspLnj9dFJWs5guJ6oTWQ0rnk8TM0130_assertion
dcterms:description
"[One of the hallmarks of Alzheimer's disease, and several other degenerative disorders such as Inclusion Body Myositis, is the abnormal accumulation of amyloid precursor protein (APP) and its proteolytic amyloid peptides.]. 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:21518451
;
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:NP460188.RASrQATiojZezdUTvspLnj9dFJWs5guJ6oTWQ0rnk8TM0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:34+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" .
}