@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP172147.RA0C4AjrznNwiOi70Xbc67EYrRF82a76BNc8SK-Fc2j-E
> .
@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:NP172147.RA0C4AjrznNwiOi70Xbc67EYrRF82a76BNc8SK-Fc2j-E130_head
{
this:
np:hasAssertion
dgn-np:NP172147.RA0C4AjrznNwiOi70Xbc67EYrRF82a76BNc8SK-Fc2j-E130_assertion
;
np:hasProvenance
dgn-np:NP172147.RA0C4AjrznNwiOi70Xbc67EYrRF82a76BNc8SK-Fc2j-E130_provenance
;
np:hasPublicationInfo
dgn-np:NP172147.RA0C4AjrznNwiOi70Xbc67EYrRF82a76BNc8SK-Fc2j-E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP172147.RA0C4AjrznNwiOi70Xbc67EYrRF82a76BNc8SK-Fc2j-E130_assertion
a
np:Assertion
.
dgn-np:NP172147.RA0C4AjrznNwiOi70Xbc67EYrRF82a76BNc8SK-Fc2j-E130_provenance
a
np:Provenance
.
dgn-np:NP172147.RA0C4AjrznNwiOi70Xbc67EYrRF82a76BNc8SK-Fc2j-E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP172147.RA0C4AjrznNwiOi70Xbc67EYrRF82a76BNc8SK-Fc2j-E130_assertion
{
miriam-gene:5621
a
ncit:C16612
.
lld:C0022336
a
ncit:C7057
.
dgn-gda:DGNab02322f3d3603b777e3d525d55a7bb5
sio:SIO_000628
miriam-gene:5621
,
lld:C0022336
;
a
sio:SIO_001121
.
}
dgn-np:NP172147.RA0C4AjrznNwiOi70Xbc67EYrRF82a76BNc8SK-Fc2j-E130_provenance
{
dgn-np:NP172147.RA0C4AjrznNwiOi70Xbc67EYrRF82a76BNc8SK-Fc2j-E130_assertion
dcterms:description
"[Alzheimer's disease (AD) and prion diseases such as sporadic Creutzfeldt-Jakob disease (sCJD) share common features concerning their molecular pathogenesis and neuropathological presentation and the coexistence of AD and CJD in patients suggest an association between the deposition of the proteolytically processed form of the amyloid precursor protein, beta-amyloid (Abeta), which deposits in AD, and the abnormal form of the prion protein, PrP(Sc), which deposits in sCJD.]. 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:18349519
;
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:NP172147.RA0C4AjrznNwiOi70Xbc67EYrRF82a76BNc8SK-Fc2j-E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:33+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" .
}